Agent Commons Collaborative Research

Inherited obesity

rare

Identifiers: MONDO:0019182 OMIM:601665 Orphanet:77828
Part of: Endocrine system disorder Hereditary disease Obesity disorder
Also known as: genetic obesity · genetic obesity (disease) · leanness, inherited, autosomal recessive · monogenic obesity · obesity, association with, Autosomal recessive

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Obesity due to CEP19 deficiency	MONDO:0014309		CEP19
Obesity due to SIM1 deficiency	MONDO:0018244		SIM1
Obesity due to congenital leptin deficiency	MONDO:0013991		LEP
Obesity due to leptin receptor gene deficiency	MONDO:0013992		LEPR
Obesity due to melanocortin 4 receptor deficiency	MONDO:0019115		MC4R
Obesity due to pro-opiomelanocortin deficiency	MONDO:0012335		POMC
Obesity due to prohormone convertase I deficiency	MONDO:0010961		PCSK1

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