oculocutaneous albinism type 1
medical condition
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oculocutaneous albinism type 1
Summary
oculocutaneous albinism type 1 is a class of disease[1]. It draws 12 Wikipedia views per month (class_of_disease category, ranking #622 of 1,968).[2]
Key Facts
- oculocutaneous albinism type 1's image is recorded as Albinistic girl papua new guinea.jpg[3].
- oculocutaneous albinism type 1's instance of is recorded as class of disease[4].
- oculocutaneous albinism type 1's subclass of is recorded as oculocutaneous albinism[5].
- oculocutaneous albinism type 1's MeSH descriptor ID is recorded as C537729[6].
- oculocutaneous albinism type 1's OMIM ID is recorded as 203100[7].
- oculocutaneous albinism type 1's OMIM ID is recorded as 606952[8].
- oculocutaneous albinism type 1's Orphanet ID is recorded as 352731[9].
- oculocutaneous albinism type 1's genetic association is recorded as monophenol monooxygenase[10].
- oculocutaneous albinism type 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_352731[11].
- oculocutaneous albinism type 1's UMLS CUI is recorded as C0268494[12].
- oculocutaneous albinism type 1's UMLS CUI is recorded as C1847024[13].
- oculocutaneous albinism type 1's ICD-10-CM is recorded as E70.3[14].
- oculocutaneous albinism type 1's GARD rare disease ID is recorded as 4037[15].
- oculocutaneous albinism type 1's Mondo ID is recorded as MONDO_0018135[16].
- oculocutaneous albinism type 1's Microsoft Academic ID is recorded as 2781331152[17].
Why It Matters
oculocutaneous albinism type 1 draws 12 Wikipedia views per month (class_of_disease category, ranking #622 of 1,968).[2]