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718605009: Congenital pontocerebellar hypoplasia type 7 (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3312895011 Congenital pontocerebellar hypoplasia type 7 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3312896012 Congenital pontocerebellar hypoplasia type 7 en Synonym Active Case insensitive SNOMED CT core
3312897015 PCH7 - pontocerebellar hypoplasia type 7 en Synonym Active Case sensitive SNOMED CT core
3312898013 Pontocerebellar hypoplasia type 7 en Synonym Active Case insensitive SNOMED CT core
3312899017 A novel very rare form of pontocerebellar hypoplasia with unknown etiology and poor prognosis reported in four patients. It has clinical characteristics in the neonatal period of hypotonia, no palpable gonads, micropenis and from infancy progressive microcephaly, apneic episodes, poor feeding, seizures and regression of penis. MRI demonstrates a pontocerebellar hypoplasia. PCH7 is expressed as PCH with 46,XY disorder of sex development in individuals with XY karyotype, and may be expressed as PCH only in individuals with XX karyotype. en Definition Active Case sensitive SNOMED CT core
3312900010 A novel very rare form of pontocerebellar hypoplasia with unknown aetiology and poor prognosis reported in four patients. It has clinical characteristics in the neonatal period of hypotonia, no palpable gonads, micropenis and from infancy progressive microcephaly, apnoeic episodes, poor feeding, seizures and regression of penis. MRI demonstrates a pontocerebellar hypoplasia. PCH7 is expressed as PCH with 46,XY disorder of sex development in individuals with XY karyotype, and may be expressed as PCH only in individuals with XX karyotype. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pontocerebellar hypoplasia type 7 Associated morphology Hypoplasia true Inferred relationship Some 1
Pontocerebellar hypoplasia type 7 Occurrence Congenital true Inferred relationship Some 1
Pontocerebellar hypoplasia type 7 Finding site Pontine structure true Inferred relationship Some 1
Pontocerebellar hypoplasia type 7 Pathological process Pathological developmental process true Inferred relationship Some 1
Pontocerebellar hypoplasia type 7 Pathological process Pathological developmental process true Inferred relationship Some 2
Pontocerebellar hypoplasia type 7 Is a Developmental hereditary disorder true Inferred relationship Some
Pontocerebellar hypoplasia type 7 Is a Congenital pontocerebellar hypoplasia true Inferred relationship Some
Pontocerebellar hypoplasia type 7 Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Pontocerebellar hypoplasia type 7 Is a Hereditary disorder of nervous system true Inferred relationship Some
Pontocerebellar hypoplasia type 7 Associated morphology Hypoplasia true Inferred relationship Some 2
Pontocerebellar hypoplasia type 7 Occurrence Congenital true Inferred relationship Some 2
Pontocerebellar hypoplasia type 7 Finding site Cerebellar structure true Inferred relationship Some 2
Pontocerebellar hypoplasia type 7 Associated morphology Hypoplasia false Inferred relationship Some 3
Pontocerebellar hypoplasia type 7 Occurrence Congenital false Inferred relationship Some 3
Pontocerebellar hypoplasia type 7 Finding site Pontine structure false Inferred relationship Some 2
Pontocerebellar hypoplasia type 7 Finding site Cerebellar structure false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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