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Summary Literature (0)
DOID:0112249 - GAPO syndrome

Disease Ontology 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.

Synonyms: growth delay-alopecia-pseudoanodontia-optic atrophy syndrome

Xenbase Genes : antxr1


MIM:
MIM:230740 - GAPO SYNDROME; GAPOS

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), syndrome (is_a)