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783703004: White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3759780013 Curatolo Cilio Pessagno syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3759781012 White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3759782017 White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3759783010 A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of severe white matter hypoplasia, corpus callosum agenesis or extreme hypoplasia, severe intellectual disability, failure to thrive and minor midline facial dysmorphism (including hypertelorism, broad nasal root, micrognathia). There have been no further descriptions in the literature since 1993. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4145661000172116 syndroom van hypoplasie van substantia alba, agenesie van corpus callosum en mentale retardatie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4145671000172113 syndroom van hypoplasie van substantia alba, agenesie van corpus callosum en verstandelijke beperking nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4145681000172111 syndroom van wittestofhypoplasie, afwezigheid van corpus callosum en verstandelijke handicap nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Is a Congenital malformation of corpus callosum true Inferred relationship Some
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Occurrence Congenital true Inferred relationship Some 3
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Occurrence Congenital true Inferred relationship Some 2
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Is a Congenital cerebellar hypoplasia true Inferred relationship Some
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Is a Genetic disease true Inferred relationship Some
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Is a Intellectual disability true Inferred relationship Some
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Occurrence Congenital true Inferred relationship Some 1
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Finding site Corpus callosum structure true Inferred relationship Some 1
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Finding site Face structure true Inferred relationship Some 2
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Associated morphology Hypoplasia true Inferred relationship Some 3
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Finding site Cerebellar white matter structure true Inferred relationship Some 3
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Associated morphology Maturation defect true Inferred relationship Some 1
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Some 4
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Has interpretation Impaired true Inferred relationship Some 4
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Interprets Adaptation behavior (observable entity) true Inferred relationship Some 5
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Has interpretation Impaired true Inferred relationship Some 5

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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