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Echinobase
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,

Echinobase Genes :


OMIM:
MIM:614120 - hydrolethalus syndrome 2; hls2

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

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