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DO Term : pontocerebellar hypoplasia type 2 [DOID:0112328] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A pontocerebellar hypoplasia characterized by pontocerebellar hypoplasia and progressive neocortical atrophy.

synonyms:
GARD:10705,
PCH2,
MESH:C548070,
ORDO:2524

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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