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715951007: Acrocallosal syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3304230017 Acrocallosal syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3304231018 Acrocallosal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3304232013 A polymalformation syndrome with main features of agenesis of corpus callosum, distal anomalies of limbs, minor craniofacial anomalies and intellectual deficit. Craniofacial anomalies include macrocephaly with protruding forehead and occiput and hypertelorism. Distal anomalies of limbs include preaxial or postaxial polydactyly or polysyndactyly of toes and/or hands. The large majority of patients have intellectual deficit that is severe in 80% of cases. Mutations of the kinesin KIF7 (15q26.1) and the transcriptional activator GLI3 (7p14.1) genes are responsible for the disease. An autosomal recessive disease. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3861931000052111 akrokalosalt syndrom sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acrocallosal syndrome (disorder) Is a Agenesis of corpus callosum true Inferred relationship Some
Acrocallosal syndrome (disorder) Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Some
Acrocallosal syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Acrocallosal syndrome (disorder) Is a Hereditary disorder of nervous system true Inferred relationship Some
Acrocallosal syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
Acrocallosal syndrome (disorder) Occurrence Congenital false Inferred relationship Some 4
Acrocallosal syndrome (disorder) Associated morphology utvecklingsabnormitet false Inferred relationship Some 5
Acrocallosal syndrome (disorder) Occurrence Congenital false Inferred relationship Some 5
Acrocallosal syndrome (disorder) Finding site Limb structure true Inferred relationship Some 3
Acrocallosal syndrome (disorder) Finding site Face structure false Inferred relationship Some 5
Acrocallosal syndrome (disorder) Associated morphology utvecklingsabnormitet false Inferred relationship Some 4
Acrocallosal syndrome (disorder) Finding site Limb structure false Inferred relationship Some 4
Acrocallosal syndrome (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 3
Acrocallosal syndrome (disorder) Finding site Entire corpus callosum false Inferred relationship Some 3
Acrocallosal syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Acrocallosal syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Acrocallosal syndrome (disorder) Finding site Entire corpus callosum true Inferred relationship Some 1
Acrocallosal syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Acrocallosal syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Acrocallosal syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Acrocallosal syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Acrocallosal syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Acrocallosal syndrome (disorder) Finding site Face structure true Inferred relationship Some 2
Acrocallosal syndrome (disorder) Associated morphology Agenesis (morphologic abnormality) true Inferred relationship Some 1
Acrocallosal syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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