ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
12 signs/symptoms

Obesity due to pro-opiomelanocortin deficiency

Oculocutaneous albinism type 2

POMC	(UniProt - OMIM)		MC1R	(UniProt - OMIM)
			OCA2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	POMC	(0.86)	MC1R

Citations in the biomedical literature:

Obesity due to pro-opiomelanocortin deficiency		Oculocutaneous albinism type 2
	Synonym(s): - POMC deficiency		Synonym(s): - OCA2

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare eye disease - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: no data available Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537730

Oculocutaneous albinism type 2
	Very frequent - Autosomal recessive inheritance - Iris albinism / ocular albinism Frequent - Abnormal pigmentary skin changes / skin pigmentation anomalies - Decreased hair pigmentation / hypopigmentation of hair - Excessive freckling - Mild visual loss / impaired visual acuity - Nystagmus - Optic nerve anomaly / optic atrophy / anomaly of the papilla - Photophobia Occasional - Melanoma - Skin / cutaneous neoplasm / tumor / carcinoma / cancer (excluding melanoma) - Strabismus / squint
Obesity due to pro-opiomelanocortin deficiency
(no data available)