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DO Term : Galloway-Mowat syndrome [DOID:0080694] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A syndrome that is characterized by developmental delay, progressive microcephaly, cerebral and cerebellar atrophy with extrapyramidal involvement, and optic atrophy.

synonyms:
ORDO:2065,
UMLS_CUI:C0795949,
GARD:65,
SNOMEDCT_US_2023_03_01:721297008,
MESH:C537548,
NCI:C132195,
PS251300,
OMIM:PS251300

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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