Disease #03799 (LEPD (obesity, severe, due to leptin deficiency (LEPD)), OMIM:614962)
Official abbreviation |
LEPD |
Name |
obesity, severe, due to leptin deficiency (LEPD) |
OMIM ID |
614962 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
LEP |
Associated tissues |
- |
Disease features |
autosomal reessive |
Remarks |
- |
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