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DO Term : congenital leptin deficiency [DOID:0111334] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • ORDO:66628,
  • OMIM:614962,
  • leptin deficiency or dysfunction,
  • obesity due to congenital leptin deficiency,
  • LEPD,
  • 614962
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents