Disease #03800 (deficiency, leptin receptor, OMIM:614963)

Official abbreviation -
Name deficiency, leptin receptor
OMIM ID 614963
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene LEPR
Associated tissues -
Disease features -
Remarks -