ODCs

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1 OMIM reference -
1 associated gene
7 signs/symptoms

PROTEIN INTERACTIONS: 1
COMMON SIGNS: 3

1 OMIM reference -
1 associated gene
16 signs/symptoms

Oculocutaneous albinism type 3

Oculocutaneous albinism type 1A


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TYRP1	(0.59)	TYR

Citations in the biomedical literature:

Oculocutaneous albinism type 3		Oculocutaneous albinism type 1A
	Synonym(s): - OCA3 - Red oculocutaneous albinism - Rufous oculocutaneous albinism - Xanthous oculocutaneous albinism		Synonym(s): - OCA1A - Tyrosinase-negative oculocutaneous albinism

	Classification (Orphanet): - Inborn errors of metabolism - Rare eye disease - Rare genetic disease - Rare skin 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: normal 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 - 2 MeSH references: C537189 / C537731		External references: 1 OMIM reference - No MeSH references


COMMON SIGNS	- Excessive freckling - Iris albinism / ocular albinism - Nystagmus

Oculocutaneous albinism type 3		Oculocutaneous albinism type 1A
	Very frequent - Abnormal pigmentary skin changes / skin pigmentation anomalies Frequent - Hair and scalp anomalies - Strabismus / squint Occasional - Skin photosensitivity		Very frequent - Autosomal recessive inheritance - Decreased hair pigmentation / hypopigmentation of hair - Diffuse / generalised skin hypopigmentation / cutaneous albinism - Macular dystrophy / absence / hypoplasia of the macula - Photophobia - Retinal albinism Frequent - Abnormal VEP / Visual evoked potential - Mild visual loss / impaired visual acuity - Optic nerve anomaly / optic atrophy / anomaly of the papilla Occasional - Corpus callosum / septum pellucidum total / partial agenesis - Hyperkeratosis / ainhum / hyperkeratotic skin fissures - Osteoporosis / osteopenia / demineralisation / osteomalacia / rickets - Skin / cutaneous neoplasm / tumor / carcinoma / cancer (excluding melanoma)