Disease #01358 (hawkinsinuria, OMIM:140350)

Official abbreviation -
Name hawkinsinuria
OMIM ID 140350
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene HPD
Associated tissues -
Disease features -
Remarks -