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Items: 2

1.

Inherited obesity

Obesity associated with an identifiable mutation in a single gene. [from NCI]

MedGen UID:
885912
Concept ID:
C4054476
Sign or Symptom
2.

Obesity due to pro-opiomelanocortin deficiency

Early-onset obesity with adrenal insuficiency and red hair (OBAIRH) is an autosomal recessive endocrine disorder characterized by early-onset obesity due to severe hyperphagia, pigmentary abnormalities, mainly pale skin and red hair, and secondary hypocortisolism. In the neonatal period, affected individuals are prone to hypoglycemia, hyperbilirubinemia, and cholestasis that may result in death if not treated. The disorder results from mutation in the POMC gene, which encodes a preproprotein that is processed into a range of bioactive peptides, including alpha-melanocyte-stimulating hormone (MSH) and ACTH (summary by Kuhnen et al., 2016 and Clement et al., 2008). [from OMIM]

MedGen UID:
341863
Concept ID:
C1857854
Disease or Syndrome

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