ZFIN Human Disease: GAPO syndrome

OBO ID: DOID:0112249

Term Name:	GAPO syndrome		Search Ontology:
Synonyms:	growth delay-alopecia-pseudoanodontia-optic atrophy syndrome
Definition:	A syndrome characterized by growth retardation, alopecia, pseudoanodontia and ocular manifestations that has_material_basis_in homozygous or compound heterozygous mutation in the ANTXR1 gene on chromosome 2p13.3. (2)
References:	OMIM:230740 ORDO:2067
Ontology:	Human Disease ( DOID:0112249 )

Relationships

is a type of:	autosomal recessive disease syndrome autosomal recessive disease syndrome Show first 5 Terms

OTHER GAPO syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ANTXR1	antxr1b antxr1d antxr1c antxr1a	GAPO syndrome	230740

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None