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Terminology chevron_right Concepts chevron_right 42357009

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Component

42357009

The component that hold information about this concept.

Fully Specified Name (FSN)

Disorder of digestive system specific to fetus or newborn (disorder)

Shortest Term

Perinatal digestive system disorders

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Disorder of digestive system specific to fetus or newborn (disorder)

SCTID: 42357009, Defined, Active

42357009|Disorder of digestive system specific to fetus or newborn (disorder)|

en Perinatal digestive system disorders
en Perinatal disorder of digestive system
en Disorder of digestive system specific to foetus or newborn
en Disorder of digestive system specific to fetus or newborn
en Disorder of digestive system specific to fetus or newborn (disorder)

Expression

42357009 |Disorder of digestive system specific to fetus or newborn (disorder)|
 === 53619000 |Disorder of digestive system (disorder)| + 
414025005 |Disorder of fetus and/or newborn (disorder)| : 
        { 246454002 |Occurrence (attribute)| = 1156676003 |Fetal and/or neonatal period (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 86762007 |Structure of digestive system (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1229853015 - Perinatal digestive system disorders (en) View
1229853015	en	Synonym (core metadata concept)	Perinatal digestive system disorders	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
70680012 - Perinatal disorder of digestive system (en) View
70680012	en	Synonym (core metadata concept)	Perinatal disorder of digestive system	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3010701014 - Disorder of digestive system specific to foetus OR newborn (en) View
3010701014	en	Synonym (core metadata concept)	Disorder of digestive system specific to foetus OR newborn	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
70677011 - Disorder of digestive system specific to fetus OR newborn (en) View
70677011	en	Synonym (core metadata concept)	Disorder of digestive system specific to fetus OR newborn	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
779247013 - Disorder of digestive system specific to fetus OR newborn (disorder) (en) View
779247013	en	Fully specified name (core metadata concept)	Disorder of digestive system specific to fetus OR newborn (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
70678018 - Disorder of digestive system specific to fetus or newborn, NOS (en) View
70678018	en	Synonym (core metadata concept)	Disorder of digestive system specific to fetus or newborn, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
70679014 - Perinatal disorder of digestive system, NOS (en) View
70679014	en	Synonym (core metadata concept)	Perinatal disorder of digestive system, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4637233022) - 42357009 -> 450426006 (246454002) View
246454002 \|Occurrence (attribute)\|	450426006 \|Fetal or neonatal period (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14912648028) - 42357009 -> 1156676003 (246454002) View
246454002 \|Occurrence (attribute)\|	1156676003 \|Fetal and/or neonatal period (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2595882020) - 42357009 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (217073020) - 42357009 -> 128122002 (116680003) View
116680003 \|Is a (attribute)\|	128122002 \|Perinatal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1766854025) - 42357009 -> 371578004 (246454002) View
246454002 \|Occurrence (attribute)\|	371578004 \|Perinatal period (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2692022029) - 42357009 -> 414025005 (116680003) View
116680003 \|Is a (attribute)\|	414025005 \|Disorder of fetus and/or newborn (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (778030022) - 42357009 -> 118971007 (363698007) View
363698007 \|Finding site (attribute)\|	118971007 \|Digestive system subdivision (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (778029028) - 42357009 -> 57855005 (246454002) View
246454002 \|Occurrence (attribute)\|	57855005 \|Perinatal state (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (217074025) - 42357009 -> 53619000 (116680003) View
116680003 \|Is a (attribute)\|	53619000 \|Disorder of digestive system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
414025005 View
414025005	Disorder of fetus and/or newborn (disorder)	Disorder of fetus or newborn	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
53619000 View
53619000	Disorder of digestive system (disorder)	Git diseases	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
206565007 View
206565007	Neonatal rumination (disorder)	Neonatal rumination	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1304114004 View
1304114004	Facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth syndrome (disorder)	Fheig syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1299153008 View
1299153008	Digenic hemochromatosis (disorder)	Digenic hemochromatosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
198626009 View
198626009	Mesenteric pregnancy (disorder)	Mesenteric pregnancy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1269271003 View
1269271003	Atypical fanconi syndrome, neonatal hyperinsulinism syndrome (disorder)	Atypical fanconi syndrome, neonatal hyperinsulinism syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1260140008 View
1260140008	Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome (disorder)	Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1220580006 View
1220580006	Isolated neonatal sclerosing cholangitis (disorder)	Isolated neonatal sclerosing cholangitis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1222706005 View
1222706005	Anterior maxillary protrusion, strabismus, intellectual disability syndrome (disorder)	Mrams syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1217380005 View
1217380005	Hypohidrosis, electrolyte imbalance, lacrimal gland dysfunction, ichthyosis, xerostomia syndrome (disorder)	Helix syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
206407004 View
206407004	Perinatal melena (disorder)	Perinatal melena	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1197033002 View
1197033002	Hereditary hemorrhagic telangiectasia of gingiva (disorder)	Hereditary hemorrhagic telangiectasia of gingiva	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1186713004 View
1186713004	Growth delay, intellectual disability, hepatopathy syndrome (disorder)	Growth delay, intellectual disability, hepatopathy syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1177081002 View
1177081002	Mulberry molar teeth (disorder)	Fournier molars	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
109436001 View
109436001	Moon molar teeth (disorder)	Bud molars	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
276563006 View
276563006	Idiopathic transient neonatal hyperinsulinemia (disorder)	Idiopathic transient neonatal hyperinsulinemia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1149069001 View
1149069001	Juvenile polyposis syndrome with hereditary hemorrhagic telangiectasia (disorder)	Juvenile polyposis syndrome with hereditary hemorrhagic telangiectasia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
65390006 View
65390006	Perinatal intestinal perforation (disorder)	Perinatal intestinal perforation	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
95555006 View
95555006	Neonatal hepatocellular damage (disorder)	Tổn thương tế bào gan sơ sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1003468008 View
1003468008	Congenital teratoma of nasopharynx (disorder)	Congenital nasopharyngeal teratoma	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
21995002 View
21995002	Natal tooth (disorder)	Natal teeth	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
109714003 View
109714003	Monostotic fibrous dysplasia of periradicular alveolar bone (disorder)	Localised periradicular osteitis fibrosa	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
253785008 View
253785008	Generalized congenital intestinal dysmotility (disorder)	Generalised intestinal dysmotility	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
63061000119104 View
63061000119104	Fetal cleft lip (disorder)	Fetal cleft lip	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
121801000119105 View
121801000119105	Fetal gastrointestinal abnormality (disorder)	Fetal gastrointestinal abnormality	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
2707005 View
2707005	Fetal and/or neonatal necrotizing inflammation of small intestine and colon (disorder)	Necrotising enterocolitis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
311808009 View
311808009	Aberrant retroesophageal subclavian artery causing dysphagia lusoria (disorder)	Aberrant retro-esophageal subclavian artery causing dysphagia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
782771007 View
782771007	Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form (disorder)	Hội chứng suy giảm dna ty thể dạng thận não gan	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
783734000 View
783734000	Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency (disorder)	Hội chứng suy giảm dna ty thể, dạng gan não do thiếu dguok	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
783738002 View
783738002	Heart defect, tongue hamartoma, polysyndactyly syndrome (disorder)	Ostravik lindemann solberg syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
783740007 View
783740007	Diazoxide-resistant focal hyperinsulinism due to sulfonylurea receptor 1 deficiency (disorder)	Tăng tiết insulin khu trú kháng diazoxide do thiếu hụt sur1	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
783741006 View
783741006	Diazoxide-resistant focal hyperinsulinism due to kir6.2 deficiency (disorder)	Tăng insulin khu trú kháng diazoxide do thiếu kir6,2	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
784346006 View
784346006	Navajo neurohepatopathy (disorder)	Navajo neuropathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1542009 View
1542009	Omphalocele with obstruction (disorder)	Irreducible omphalocele	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
36631002 View
36631002	Hepatomphalocele (disorder)	Hepatomphalocele	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
47028006 View
47028006	Congenital hiatus hernia (disorder)	Congenital hiatal hernia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
198273008 View
198273008	Congenital vaginal enterocele (disorder)	Congenital vaginal enterocele	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
770944002 View
770944002	Oculootodental syndrome (disorder)	Oculootodental syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
773415005 View
773415005	Contiguous abcd1 dxs1357e deletion syndrome (disorder)	Hội chứng xóa abcd1 dxs1357e liền kề	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
773579007 View
773579007	Congenital chronic diarrhea with protein-losing enteropathy (disorder)	Congenital chronic diarrhea with exudative enteropathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
773666007 View
773666007	Hypoinsulinemic hypoglycemia and body hemihypertrophy (disorder)	Hạ đường huyết giảm insulin máu và phì đại nửa người	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
764962002 View
764962002	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder)	Bệnh não gan do khiếm khuyết kết hợp phosphoryl hóa oxy hóa typ 1	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
735496003 View
735496003	Transient neonatal hypoglycemia due to hyperinsulinemia (disorder)	Transient hyperinsulinemic neonatal hypoglycemia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
735677007 View
735677007	Neonatal hemorrhage of liver (disorder)	Xuất huyết gan trẻ sơ sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
737211006 View
737211006	Neonatal disorder of oral mucosa (disorder)	Neonatal disorder of oral mucosa	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
746223006 View
746223006	Neonatal infection of mouth caused by candida (disorder)	Neonatal oral thrush	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
723442008 View
723442008	Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome (disorder)	Stoelinga de koomen davis syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
724276006 View
724276006	X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome (disorder)	Autoimmune enteropathy type 1	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
724361001 View
724361001	Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder)	Vodi syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
733071009 View
733071009	Deafness, small bowel diverticulosis, neuropathy syndrome (disorder)	Groll hirschowitz syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
719687007 View
719687007	Gingival fibromatosis with facial dysmorphism syndrome (disorder)	Gingival fibromatosis with facial dysmorphism syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
720980004 View
720980004	Alopecia, psychomotor epilepsy, periodontal pyorrhea, intellectual disability syndrome (disorder)	Shokeir syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
721154006 View
721154006	Congenital chalasia of esophagus (disorder)	Congenital chalasia of esophagus	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
721236002 View
721236002	Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme a dehydrogenase deficiency (disorder)	Hyperinsulinism due to short chain 3-hydroxylacyl-coa dehydrogenase deficiency	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
721646008 View
721646008	Congenital diverticulitis of small intestine (disorder)	Congenital diverticulitis of small intestine	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
721834007 View
721834007	Hyperinsulinism due to uncoupling protein 2 deficiency (disorder)	Hyperinsulinism due to ucp2 deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722034006 View
722034006	Median nodule of upper lip (disorder)	Median nodule of upper lip	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722207000 View
722207000	Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder)	Hội chứng suy tụy, thiếu máu do loạn sản hồng cầu, phì đại xương sọ	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722288007 View
722288007	Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome (disorder)	Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722377004 View
722377004	Paraganglioma and gastric stromal sarcoma syndrome (disorder)	Carney stratakis dyad	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722392003 View
722392003	Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder)	Enteric anendocrinosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722916005 View
722916005	Neonatal hypotonia of hypopharynx (disorder)	Neonatal hypotonia of hypopharynx	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
723111007 View
723111007	Neonatal mass of hypopharynx (disorder)	U hạ họng sơ sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
716092007 View
716092007	Radial hypoplasia and triphalangeal thumb with hypospadias and maxillary diastema syndrome (disorder)	Schmitt gillenwater kelly syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
716180009 View
716180009	Odontoma dysphagia syndrome (disorder)	Boder syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
716277000 View
716277000	Chronic diarrhea due to glucoamylase deficiency (disorder)	Maltase glucoamylase deficiency	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
717046003 View
717046003	Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency (disorder)	Autosomal dominant hyperinsulinism due to sur1 deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
717053007 View
717053007	Renal tubulopathy with encephalopathy and liver failure syndrome (disorder)	Renal tubulopathy with encephalopathy and liver failure syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
717155003 View
717155003	Neonatal intrahepatic cholestasis due to citrin deficiency (disorder)	Ứ mật trong gan do thiếu citrin sơ sinh	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
717182006 View
717182006	Hyperinsulinism due to deficiency of glucokinase (disorder)	Tăng tiết insulin do thiếu glucokinase	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
718106009 View
718106009	Hyperinsulinism and hyperammonemia syndrome (disorder)	Hội chứng tăng insulin và tăng urê huyết	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
86443005 View
86443005	Hutchinson's teeth (disorder)	Hutchinson teeth	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
204788008 View
204788008	Congenital atrophy of left lobe of liver (disorder)	Teo thùy gan trái bẩm sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
235913009 View
235913009	Congenital disorder of gallbladder and biliary tract (disorder)	Rối loạn bẩm sinh của túi mật và đường mật	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
700283004 View
700283004	Congenital achalasia of esophagus (disorder)	Congenital achalasia of esophagus	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
700285006 View
700285006	Congenital incomplete closure of velopharyngeal apparatus (disorder)	Loạn năng vòm hầu bẩm sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
702364003 View
702364003	Chylomicron retention disease (disorder)	Anderson syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
450849003 View
450849003	Congenital monosaccharide malabsorption (disorder)	Congenital monosaccharide malabsorption	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
48729005 View
48729005	Perinatal gastrointestinal hemorrhage (disorder)	Perinatal gastrointestinal hemorrhage	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
84752003 View
84752003	Mottled teeth, congenital (disorder)	Mottled tooth	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
276521007 View
276521007	Perinatal intestinal obstruction (disorder)	Perinatal intestinal obstruction	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
433237003 View
433237003	Cholestasis in newborn (disorder)	Ứ mật ở trẻ sơ sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
58748004 View
58748004	Neonatal tooth (disorder)	Neonatal tooth	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
80378000 View
80378000	Neonatal hepatosplenomegaly (disorder)	Gan lách to sơ sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
196279002 View
196279002	Neonatal enamel hypoplasia (disorder)	Neonatal enamel hypoplasia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
206424005 View
206424005	Neonatal melena (disorder)	Neonatal melena	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
57341009 View
57341009	Meconium peritonitis (disorder)	Meconium peritonitis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
276548008 View
276548008	Perinatal disorders of liver and/or biliary system (disorder)	Perinatal disorders of liver and biliary system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363219007 View
363219007	Neonatal gastrointestinal disorder (disorder)	Neonatal gastrointestinal disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
69800000 View
69800000	Neonatal hepatitis (disorder)	Viêm gan sơ sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
62216007 View
62216007	Familial arthrogryposis-cholestatic hepatorenal syndrome (disorder)	Hội chứng gan thận ứ mật - cứng khớp gia đình	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
206372007 View
206372007	Congenital viral hepatitis (disorder)	Viêm gan virus bẩm sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
6075009 View
6075009	Glycogen storage disease, hepatic form (disorder)	Bệnh dự trữ glycogen, thể gan	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
7037003 View
7037003	Xeroderma, talipes and enamel defect syndrome (disorder)	Xte syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
8933000 View
8933000	Crigler-najjar syndrome, type i (disorder)	Crigler-najjar type 1	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
25898005 View
25898005	Congenital secretory diarrhea (disorder)	Congenital secretory diarrhea	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
28212002 View
28212002	Intestinal lipofuscinosis (disorder)	Brown bowel syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
30188007 View
30188007	Alpha-1-antitrypsin deficiency (disorder)	Thiếu alpha-1-antitrypsin	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
32891000 View
32891000	Rotor syndrome (disorder)	Rotor syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
50869007 View
50869007	Ehlers-danlos syndrome, type 8 (disorder)	Ehlers-danlos syndrome type 8	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
54411001 View
54411001	Peutz-jeghers syndrome (disorder)	Perioral lentiginosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
56661000 View
56661000	Intestinal enteropeptidase deficiency (disorder)	Congenital enterokinase deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
63702009 View
63702009	Alstrom syndrome (disorder)	Alstrom syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
69478001 View
69478001	Pancreatic colipase deficiency (disorder)	Thiếu colipase tuyến tụy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
69518005 View
69518005	Congenital anomaly of digestive system (disorder)	Congenital anomaly of digestive system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
70737009 View
70737009	Mucopolysaccharidosis, mps-ii (disorder)	Hunter disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
78960005 View
78960005	Pancreatic triacylglycerol lipase deficiency (disorder)	Isolated lipase deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
89454001 View
89454001	Shwachman syndrome (disorder)	Shwachman syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
204670005 View
204670005	Congenital pyloric spasm (disorder)	Congenital pylorospasm	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
235908005 View
235908005	Glycogen phosphorylase kinase deficiency (disorder)	Glycogenosis viiia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
235915002 View
235915002	Synthetic defect of bile acids (disorder)	Bile acid synthetic defect	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
237964009 View
237964009	Glycogen synthase deficiency (disorder)	Thiếu hụt glycogen synthase	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
253758001 View
253758001	Congenital palatoesophageal incoordination (disorder)	Nasopharyngeal dysmotility	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
253767001 View
253767001	Congenital functional disorders of the small intestine (disorder)	Congenital functional disorders of the small intestine	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
253778009 View
253778009	Congenital functional disorders of the colon (disorder)	Congenital functional disorders of the colon	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
268245001 View
268245001	Harlequin fetus (disorder)	Harlequin fetus	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

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ExtendedMap object (bbc69e82-3ebf-57b2-be64-9592c1bfa97d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	P78.9	TRUE	ALWAYS P78.9	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|

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