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38353004: Congenital porencephaly (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
63417013 Congenital porencephaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
63419011 Congenital porencephalia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
63420017 Congenital cerebral porosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
63421018 Schizencephalic porencephaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
773333019 Congenital porencephaly (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
508771000172117 porencéphalie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital porencephaly Is a Congenital anomaly of brain true Inferred relationship Some
Congenital porencephaly Finding site Structure of central nervous system (body structure) false Inferred relationship Some 1
Congenital porencephaly Associated morphology anomalie du développement false Inferred relationship Some 1
Congenital porencephaly Occurrence Congenital false Inferred relationship Some
Congenital porencephaly Associated morphology Congenital cavitation false Inferred relationship Some 1
Congenital porencephaly Finding site Brain structure true Inferred relationship Some 1
Congenital porencephaly Is a Congenital malformation false Inferred relationship Some
Congenital porencephaly Finding site Brain structure false Inferred relationship Some 1
Congenital porencephaly Associated morphology Congenital cavitation false Inferred relationship Some 1
Congenital porencephaly Occurrence Congenital false Inferred relationship Some 2
Congenital porencephaly Associated morphology anomalie du développement false Inferred relationship Some 2
Congenital porencephaly Finding site Brain structure false Inferred relationship Some 2
Congenital porencephaly Occurrence Congenital false Inferred relationship Some 3
Congenital porencephaly Finding site Brain structure false Inferred relationship Some 3
Congenital porencephaly Associated morphology Congenital cavitation false Inferred relationship Some 3
Congenital porencephaly Occurrence Congenital true Inferred relationship Some 1
Congenital porencephaly Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital porencephaly Is a Congenital and developmental anomalies of the nervous system false Inferred relationship Some
Congenital porencephaly Associated morphology Cystic dilatation true Inferred relationship Some 1
Congenital porencephaly Is a Lesion of brain true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Porencephaly-cerebellar hypoplasia-internal malformations syndrome is rare central nervous system malformation syndrome characterised by bilateral porencephaly, absence of the septum pellucidum and cerebellar hypoplasia with absent vermis. Additionally, dysmorphic facial features (hypertelorism, epicanthic folds, high arched palate, prominent metopic suture), macrocephaly, corneal clouding, situs inversus, tetralogy of Fallot, atrial septal defects and/or seizures have been observed. Is a True Congenital porencephaly Inferred relationship Some
A rare, genetic, central nervous system malformation syndrome characterized by bilateral congenital cataracts and severe hemorrhagic destruction of the brain parenchyma with associated massive cystic degeneration, enlarged ventricles and subependymal calcification. Patients typically present generalized spasticity, increased deep tendon reflexes and seizures. Hepatomegaly and renal anomalies have also been reported. Is a True Congenital porencephaly Inferred relationship Some

This concept is not in any reference sets

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