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DO Term : PEHO syndrome [DOID:0080539] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A brain disease that is characterized by extreme cerebellar atrophy due to almost total granule neuron loss.

synonyms:
OMIM:260565,
ORDO:2836,
260565,
MESH:C536317,
GARD:4264

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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