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 22 genes , ADRB2, ADRB3, AGRP, CARTPT, ENPP1, GHRL, KANK1, LEPR, MC4R, more than 10, MRAP2, MT-CYB, NR0B2, POMC, PPARG, PPARGC1B, PYY, SDC3, SIM1, UCP1, UCP3
Associated tissues -
Disease features -
Remarks -

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