Disease #00114

Official abbreviation 601665
Name Obesity, autosomal dominant, 601665 (3)
OMIM ID 601665
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 15 genes -, ADRB2, ADRB3, CARTPT, ENPP1, GHRL, KANK1, LEPR, MC4R, more than 10, MRAP2, MT-CYB, PYY, UCP1, UCP3
Associated tissues -
Disease features -
Remarks -