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DOID:0111590 - Cohen syndrome
Disease Ontology Definition:A syndrome characterized by facial dysmorphism, microcephaly, truncal obesity, impaired intellectual development, progressive retinopathy, and intermittent congenital neutropenia that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13B gene on chromosome 8q22.2.
Synonyms: COH1, Hypotonia, obesity, and prominent incisors, Pepper syndrome
Xenbase Genes
:
vps13b
| MIM:216550 - COHEN SYNDROME; COH1 |
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)