Search Ontology:
Human Disease

Galloway-Mowat syndrome

Term ID
DOID:0080694
Synonyms
Definition
A syndrome that is characterized by developmental delay, progressive microcephaly, cerebral and cerebellar atrophy with extrapyramidal involvement, and optic atrophy. (3)
References
Ontology
Human Disease   ( DOID:0080694 )
Relationships
is a type of
has subtype
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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