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718609003: Congenital pontocerebellar hypoplasia type 3 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3312920011 Congenital pontocerebellar hypoplasia type 3 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312921010 Congenital pontocerebellar hypoplasia type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312922015 PCH3 - pontocerebellar hypoplasia type 3 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3312923013 Pontocerebellar hypoplasia type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312924019 Cerebellar atrophy with progressive microcephaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312925018 A rare form of PCH with clinical manifestation neonatally of hypotonia and impaired swallowing and from infancy onward seizures, optic atrophy and short stature, but none of the clinical findings are specific for PCH3. To date, PCH3 is reported in only 3 families. In 2 families, an implication of locus 7q11-21 has been demonstrated. PCH3 is inherited in an autosomal recessive manner. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital pontocerebellar hypoplasia type 3 (disorder) Is a Congenital pontocerebellar hypoplasia true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 3 (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 3 (disorder) Is a Hereditary disorder of nervous system true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 3 (disorder) Associated morphology Hypoplasia true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 3 (disorder) Occurrence Congenital true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 3 (disorder) Finding site Cerebellar structure true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 3 (disorder) Associated morphology Hypoplasia false Inferred relationship Some 3
Congenital pontocerebellar hypoplasia type 3 (disorder) Occurrence Congenital false Inferred relationship Some 3
Congenital pontocerebellar hypoplasia type 3 (disorder) Finding site Pontine structure false Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 3 (disorder) Finding site Cerebellar structure false Inferred relationship Some 3
Congenital pontocerebellar hypoplasia type 3 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 3 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 3 (disorder) Associated morphology Hypoplasia true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 3 (disorder) Finding site Pontine structure true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 3 (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 3 (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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