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Summary Literature (0)
DOID:0111356 - hydrolethalus syndrome 2

Disease Ontology Definition:A hydrolethalus syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the KIF7 gene on chromosome 15q26.1.

Synonyms: HLS2

Xenbase Genes : kif7


MIM:
MIM:614120 - HYDROLETHALUS SYNDROME 2; HLS2

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

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