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 |
- |
|