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Terminology chevron_right Concepts chevron_right 770678005

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770678005
The component that hold information about this concept.
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (disorder)
Peho-like syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (disorder)

SCTID: 770678005, Primitive, Active


770678005|Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (disorder)|
  • en Peho-like syndrome
  • en Pehol (progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like) syndrome
  • en Pehol (progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like) syndrome
  • en Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome
  • en Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (disorder)
  • en Progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like syndrome

770678005 |Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (disorder)|

<<< 78689005 |Chronic brain syndrome (disorder)| +
    52522001 |Degenerative brain disorder (disorder)| +
    128613002 |Seizure disorder (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    106018006 |Hereditary degenerative disease of central nervous system (disorder)| +
    118654009 |Disorder characterized by edema (disorder)| +
    118930001 |Disorder of face (disorder)| +
    128605003 |Disorder of extremity (disorder)| +
    424372002 |Edema of extremity (finding)| +
    445088006 |Edema of face (finding)| :
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 79654002 |Edema (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 66019005 |Limb structure (body structure)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 79654002 |Edema (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 89545001 |Face structure (body structure)| }
Active

3702073010 - PEHO-like syndrome (en) View

3702073010
en
Synonym (core metadata concept)
PEHO-like syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

3702078018 - PEHOL (progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like) syndrome (en) View

3702078018
en
Synonym (core metadata concept)
PEHOL (progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like) syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

3702080012 - PEHOL (progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like) syndrome (en) View

3702080012
en
Synonym (core metadata concept)
PEHOL (progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like) syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

3702076019 - Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (en) View

3702076019
en
Synonym (core metadata concept)
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3702075015 - Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (disorder) (en) View

3702075015
en
Fully specified name (core metadata concept)
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3702074016 - Progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like syndrome (en) View

3702074016
en
Synonym (core metadata concept)
Progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (9618050024) - 770678005 -> 280369009 (363698007) View

363698007 |Finding site (attribute)|
280369009 |Brain tissue structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (15805424024) - 770678005 -> 12738006 (363698007) View

363698007 |Finding site (attribute)|
12738006 |Brain structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9618045029) - 770678005 -> 254199006 (116680003) View

116680003 |Is a (attribute)|
254199006 |Hereditary lymphedema (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (9618052027) - 770678005 -> 30213001 (116676008) View

116676008 |Associated morphology (attribute)|
30213001 |Lymphatic edema (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (15143704028) - 770678005 -> 118654009 (116680003) View

116680003 |Is a (attribute)|
118654009 |Disorder characterized by edema (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15143705027) - 770678005 -> 118930001 (116680003) View

116680003 |Is a (attribute)|
118930001 |Disorder of face (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15143706026) - 770678005 -> 128605003 (116680003) View

116680003 |Is a (attribute)|
128605003 |Disorder of extremity (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15143707024) - 770678005 -> 424372002 (116680003) View

116680003 |Is a (attribute)|
424372002 |Edema of extremity (finding)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15143708025) - 770678005 -> 445088006 (116680003) View

116680003 |Is a (attribute)|
445088006 |Edema of face (finding)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15143709022) - 770678005 -> 66019005 (363698007) View

363698007 |Finding site (attribute)|
66019005 |Limb structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15143710028) - 770678005 -> 79654002 (116676008) View

116676008 |Associated morphology (attribute)|
79654002 |Edema (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15143711029) - 770678005 -> 89545001 (363698007) View

363698007 |Finding site (attribute)|
89545001 |Face structure (body structure)|
4
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15143712020) - 770678005 -> 79654002 (116676008) View

116676008 |Associated morphology (attribute)|
79654002 |Edema (morphologic abnormality)|
4
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9618046028) - 770678005 -> 33359002 (116676008) View

116676008 |Associated morphology (attribute)|
33359002 |Degeneration (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (9618051023) - 770678005 -> 363235000 (116680003) View

116680003 |Is a (attribute)|
363235000 |Hereditary disorder of nervous system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (12094906029) - 770678005 -> 106018006 (116680003) View

116680003 |Is a (attribute)|
106018006 |Hereditary degenerative disease of central nervous system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12094907022) - 770678005 -> 107669003 (116676008) View

116676008 |Associated morphology (attribute)|
107669003 |Degenerative abnormality (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9618054026) - 770678005 -> 255314001 (263502005) View

263502005 |Clinical course (attribute)|
255314001 |Progressive (qualifier value)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9618047021) - 770678005 -> 78689005 (116680003) View

116680003 |Is a (attribute)|
78689005 |Chronic brain syndrome (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9618048027) - 770678005 -> 52522001 (116680003) View

116680003 |Is a (attribute)|
52522001 |Degenerative brain disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9618049024) - 770678005 -> 128613002 (116680003) View

116680003 |Is a (attribute)|
128613002 |Seizure disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9618053021) - 770678005 -> 85995004 (116680003) View

116680003 |Is a (attribute)|
85995004 |Autosomal recessive hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

106018006 View

106018006
Hereditary degenerative disease of central nervous system (disorder)
Hereditary degenerative disease of central nervous system
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

445088006 View

445088006
Edema of face (finding)
Phù mặt
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

424372002 View

424372002
Edema of extremity (finding)
Edema of extremity
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

52522001 View

52522001
Degenerative brain disorder (disorder)
Cerebral degeneration
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

128613002 View

128613002
Seizure disorder (disorder)
Bệnh co giật
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

78689005 View

78689005
Chronic brain syndrome (disorder)
Chronic brain syndrome
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

118654009 View

118654009
Disorder characterized by edema (disorder)
Disorder characterized by edema
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

118930001 View

118930001
Disorder of face (disorder)
Disease of face
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

128605003 View

128605003
Disorder of extremity (disorder)
Disorder of limb
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (65c59df2-21a6-5824-9a41-859d7c4a9a13) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G31.8
TRUE
ALWAYS G31.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
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 (c2a8360e-5669-5252-b0b5-f5e7893dd25e) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G93.4
TRUE
ALWAYS G93.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
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)|
esc