oculocutaneous albinism
(Q2017741)
autosomal recessive disease characterized by abnormal pigmentation of the skin, hair and eyes
autosomal recessive disease characterized by abnormal pigmentation of the skin, hair and eyes
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Current Data About
oculocutaneous albinism
| (P31) |
(Q42303753)
(Q929833) (Q112193867) |
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| (P279) |
(Q10267817)
(Q81867) |
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| (P1325) |
http://www.nanbyou.or.jp/entry/4492
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| (P1692) |
270.2
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| (P1748) |
C84941
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| (P1995) |
(Q161437)
(Q171171) |
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| (P2293) |
(Q14916171)
(Q18030258)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_0050632
http://identifiers.org/doid/DOID:0050632
http://www.orpha.net/ORDO/Orphanet_55 |
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| (P5008) |
(Q4099686)
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other details
| aliases |
Albinism, Oculocutaneous OCA |
| description | autosomal recessive disease characterized by abnormal pigmentation of the skin, hair and eyes |
External Links