ZFIN Human Disease: Galloway-Mowat syndrome

OBO ID: DOID:0080694

Term Name:	Galloway-Mowat syndrome		Search Ontology:
Synonyms:
Definition:	A syndrome that is characterized by developmental delay, progressive microcephaly, cerebral and cerebellar atrophy with extrapyramidal involvement, and optic atrophy. (3)
References:	GARD:65 MESH:C537548 NCI:C132195 OMIM:PS251300 ORDO:2065 SNOMEDCT_US_2023_03_01:721297008 UMLS_CUI:C0795949
Ontology:	Human Disease ( DOID:0080694 )

Relationships

is a type of:	syndrome syndrome Show first 5 Terms
has subtype:	Galloway-Mowat syndrome 1 Galloway-Mowat syndrome 2 Galloway-Mowat syndrome 3 Galloway-Mowat syndrome 4 Galloway-Mowat syndrome 5 Galloway-Mowat syndrome 1 Galloway-Mowat syndrome 2 Galloway-Mowat syndrome 3 Galloway-Mowat syndrome 4 Galloway-Mowat syndrome 5 Show first 5 Terms

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Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None