Term Name:	congenital leptin deficiency
Synonyms:	LEPD, leptin deficiency or dysfunction, obesity due to congenital leptin deficiency
Definition:	A syndrome characterized by severe early-onset obesity, hyperphagia, hypogonadotropic hypogonadism, and neuroendocrine and metabolic dysfunction that has_material_basis_in homozygous or compound heterozygous mutation in LEP on chromosome 7q32.1.
Ontology:	Human Disease [DOID:0111334]   ( DOID:0111334 )