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pro-opiomelanocortin (POMC) deficiency

Genetics: - associated with defects in POMC Clinical manifestations: - early-onset obesity - adrenal insufficiency - red hair - pale skin

Related

pro-opiomelanocortin; corticotropin-lipotropin (POMC)

General

genetic disease of the endocrine system

Database Correlations

OMIM 609734

References

  1. OMIM :accession 609734
  2. NEJM Knowledge+ Endocrinology