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Terminology chevron_right Concepts chevron_right 56212008

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Component

56212008

The component that hold information about this concept.

Fully Specified Name (FSN)

Leydig cell agenesis (disorder)

Shortest Term

Leydig cell agenesis

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

Leydig cell agenesis (disorder)

SCTID: 56212008, Defined, Active

56212008|Leydig cell agenesis (disorder)|

en Leydig cell hypoplasia
en Gonadotrophin unresponsiveness syndrome
en Gonadotropin unresponsiveness syndrome
en Leydig cell agenesis (disorder)
en Leydig cell agenesis
en Leydig cell dysgenesis

Expression

56212008 |Leydig cell agenesis (disorder)|
 === 363070008 |Developmental hereditary disorder (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
85437001 |Congenital hypoplasia of testis (disorder)| + 
363104002 |Hereditary disorder of endocrine system (disorder)| + 
371122009 |Congenital anomaly of endocrine testis (disorder)| + 
363039000 |Congenital connective tissue disorder (disorder)| + 
363045008 |Connective tissue hereditary disorder (disorder)| + 
363290007 |Reproductive system hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 44185004 |Structure of interstitial cell of leydig (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3752705016 - Leydig cell hypoplasia (en) View
3752705016	en	Synonym (core metadata concept)	Leydig cell hypoplasia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
93484018 - Gonadotrophin unresponsiveness syndrome (en) View
93484018	en	Synonym (core metadata concept)	Gonadotrophin unresponsiveness syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
93482019 - Gonadotropin unresponsiveness syndrome (en) View
93482019	en	Synonym (core metadata concept)	Gonadotropin unresponsiveness syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
794700014 - Leydig cell agenesis (disorder) (en) View
794700014	en	Fully specified name (core metadata concept)	Leydig cell agenesis (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
93481014 - Leydig cell agenesis (en) View
93481014	en	Synonym (core metadata concept)	Leydig cell agenesis	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
93483012 - Leydig cell dysgenesis (en) View
93483012	en	Synonym (core metadata concept)	Leydig cell dysgenesis	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11538370029) - 56212008 -> 363044007 (116680003) View
116680003 \|Is a (attribute)\|	363044007 \|Connective tissue disorder by body site (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13069674022) - 56212008 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5000530024) - 56212008 -> 280133005 (116680003) View
116680003 \|Is a (attribute)\|	280133005 \|Disorder of soft tissue of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2670955023) - 56212008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5000528022) - 56212008 -> 274151005 (116680003) View
116680003 \|Is a (attribute)\|	274151005 \|Congenital absence of testis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10514470020) - 56212008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11151622023) - 56212008 -> 363045008 (116680003) View
116680003 \|Is a (attribute)\|	363045008 \|Connective tissue hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11151623029) - 56212008 -> 363290007 (116680003) View
116680003 \|Is a (attribute)\|	363290007 \|Reproductive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11151624024) - 56212008 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11151625020) - 56212008 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11151626021) - 56212008 -> 85437001 (116680003) View
116680003 \|Is a (attribute)\|	85437001 \|Congenital hypoplasia of testis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11151627028) - 56212008 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3429425023) - 56212008 -> 44185004 (363698007) View
363698007 \|Finding site (attribute)\|	44185004 \|Structure of interstitial cell of leydig (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4980200029) - 56212008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5000531023) - 56212008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5000532027) - 56212008 -> 367715001 (363698007) View
363698007 \|Finding site (attribute)\|	367715001 \|Entire interstitial cell of leydig (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6079806021) - 56212008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5000527028) - 56212008 -> 239953001 (116680003) View
116680003 \|Is a (attribute)\|	239953001 \|Lesion of soft tissue (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (813417029) - 56212008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3460503024) - 56212008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3601112021) - 56212008 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3601113027) - 56212008 -> 71934003 (363698007) View
363698007 \|Finding site (attribute)\|	71934003 \|Genital structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3601114022) - 56212008 -> 304042006 (363698007) View
363698007 \|Finding site (attribute)\|	304042006 \|Testicular endocrine structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3609701028) - 56212008 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4740169024) - 56212008 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4740170020) - 56212008 -> 12921003 (363698007) View
363698007 \|Finding site (attribute)\|	12921003 \|Pelvic structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5000529025) - 56212008 -> 363039000 (116680003) View
116680003 \|Is a (attribute)\|	363039000 \|Congenital connective tissue disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3535569022) - 56212008 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3535570023) - 56212008 -> 71934003 (363698007) View
363698007 \|Finding site (attribute)\|	71934003 \|Genital structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3556115028) - 56212008 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3556116027) - 56212008 -> 304042006 (363698007) View
363698007 \|Finding site (attribute)\|	304042006 \|Testicular endocrine structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2548669028) - 56212008 -> 363039000 (116680003) View
116680003 \|Is a (attribute)\|	363039000 \|Congenital connective tissue disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2548670027) - 56212008 -> 239990000 (116680003) View
116680003 \|Is a (attribute)\|	239990000 \|Soft tissue lesion of pelvic region (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2771248022) - 56212008 -> 274151005 (116680003) View
116680003 \|Is a (attribute)\|	274151005 \|Congenital absence of testis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (813423023) - 56212008 -> 44185004 (363698007) View
363698007 \|Finding site (attribute)\|	44185004 \|Structure of interstitial cell of leydig (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2670954022) - 56212008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1771311029) - 56212008 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1771312020) - 56212008 -> 127943004 (363698007) View
363698007 \|Finding site (attribute)\|	127943004 \|Entire endocrine testis (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (239537022) - 56212008 -> 73465006 (116680003) View
116680003 \|Is a (attribute)\|	73465006 \|Congenital absence of germinal epithelium of testes (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (529767029) - 56212008 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (813424028) - 56212008 -> 53472008 (363698007) View
363698007 \|Finding site (attribute)\|	53472008 \|Structure of spermatogenic epithelium (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2268178023) - 56212008 -> 118975003 (363698007) View
363698007 \|Finding site (attribute)\|	118975003 \|Entire subdivision of male genital system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2771249025) - 56212008 -> 371122009 (116680003) View
116680003 \|Is a (attribute)\|	371122009 \|Congenital anomaly of endocrine testis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2268177029) - 56212008 -> 128181006 (363698007) View
363698007 \|Finding site (attribute)\|	128181006 \|Entire genital organ (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2268179026) - 56212008 -> 40689003 (363698007) View
363698007 \|Finding site (attribute)\|	40689003 \|Testis structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2455005021) - 56212008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2523471028) - 56212008 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2527889022) - 56212008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (813418023) - 56212008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1677944024) - 56212008 -> 105969002 (116680003) View
116680003 \|Is a (attribute)\|	105969002 \|Disorder of connective tissue (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2451755027) - 56212008 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2207867022) - 56212008 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2215856026) - 56212008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1771310028) - 56212008 -> 90264002 (363698007) View
363698007 \|Finding site (attribute)\|	90264002 \|Male genital structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2201235022) - 56212008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1708879027) - 56212008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (239536029) - 56212008 -> 19660004 (116680003) View
116680003 \|Is a (attribute)\|	19660004 \|Disorder of soft tissue (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (239538028) - 56212008 -> 362969004 (116680003) View
116680003 \|Is a (attribute)\|	362969004 \|Disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (529769026) - 56212008 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (529770025) - 56212008 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (529772022) - 56212008 -> 71934003 (363698007) View
363698007 \|Finding site (attribute)\|	71934003 \|Genital structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (813419026) - 56212008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (813422029) - 56212008 -> 211384000 (260908002) View
260908002 \|Course (attribute)\|	211384000 \|Multiple superficial injuries of lower leg (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363039000 View
363039000	Congenital connective tissue disorder (disorder)	Congenital connective tissue disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363045008 View
363045008	Connective tissue hereditary disorder (disorder)	Connective tissue hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
371122009 View
371122009	Congenital anomaly of endocrine testis (disorder)	Congenital anomaly of endocrine testis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85437001 View
85437001	Congenital hypoplasia of testis (disorder)	Streak testis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363104002 View
363104002	Hereditary disorder of endocrine system (disorder)	Hereditary disorder of endocrine system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363290007 View
363290007	Reproductive system hereditary disorder (disorder)	Reproductive system hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1003437009 View
1003437009	Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder)	Leydig cell hypoplasia due to complete lh receptor inactivation	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1003438004 View
1003438004	Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation (disorder)	Leydig cell hypoplasia due to partial lh receptor inactivation	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (aa20a42e-a5f0-5dcf-92a2-6c05c395a2b9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q55.0	TRUE	ALWAYS Q55.0	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)\|
ExtendedMap object (fd79bb70-3200-5170-b602-6df218570a21) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E29.1	TRUE	ALWAYS E29.1 \| POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE	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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