Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Oculocutaneous_albinism_type_I> ?p ?o }
Showing triples 1 to 37 of
37
with 100 triples per page.
- Oculocutaneous_albinism_type_I abstract "Oculocutaneous Albinism Type I or –Type 1A (OCA1A) is an autosomal recessive skin disease associated with albinism. This type of albinism is caused when the gene OCA1 does not function properly.The location of OCA1 may be written as \"11q1.4-q2.1\", meaning it is on chromosome 11, long arm, somewhere in the range of band 1, sub-band 4, and band 2, sub-band 1.".
- Oculocutaneous_albinism_type_I omim "203100".
- Oculocutaneous_albinism_type_I wikiPageID "18842173".
- Oculocutaneous_albinism_type_I wikiPageLength "943".
- Oculocutaneous_albinism_type_I wikiPageOutDegree "9".
- Oculocutaneous_albinism_type_I wikiPageRevisionID "654888067".
- Oculocutaneous_albinism_type_I wikiPageWikiLink Albinism.
- Oculocutaneous_albinism_type_I wikiPageWikiLink Autosome.
- Oculocutaneous_albinism_type_I wikiPageWikiLink Category:Autosomal_recessive_disorders.
- Oculocutaneous_albinism_type_I wikiPageWikiLink Chromosome.
- Oculocutaneous_albinism_type_I wikiPageWikiLink Chromosome_11_(human).
- Oculocutaneous_albinism_type_I wikiPageWikiLink Cutaneous_condition.
- Oculocutaneous_albinism_type_I wikiPageWikiLink Dominance_(genetics).
- Oculocutaneous_albinism_type_I wikiPageWikiLink Locus_(genetics).
- Oculocutaneous_albinism_type_I wikiPageWikiLink OCA1_(gene).
- Oculocutaneous_albinism_type_I wikiPageWikiLinkText "Oculocutaneous albinism type I".
- Oculocutaneous_albinism_type_I name "Oculocutaneous albinism type I".
- Oculocutaneous_albinism_type_I omim "203100".
- Oculocutaneous_albinism_type_I wikiPageUsesTemplate Template:Genetic-disorder-stub.
- Oculocutaneous_albinism_type_I wikiPageUsesTemplate Template:Infobox_disease.
- Oculocutaneous_albinism_type_I wikiPageUsesTemplate Template:Reflist.
- Oculocutaneous_albinism_type_I subject Category:Autosomal_recessive_disorders.
- Oculocutaneous_albinism_type_I hypernym Disease.
- Oculocutaneous_albinism_type_I type Disease.
- Oculocutaneous_albinism_type_I type Disorder.
- Oculocutaneous_albinism_type_I type Thing.
- Oculocutaneous_albinism_type_I type Q12136.
- Oculocutaneous_albinism_type_I comment "Oculocutaneous Albinism Type I or –Type 1A (OCA1A) is an autosomal recessive skin disease associated with albinism. This type of albinism is caused when the gene OCA1 does not function properly.The location of OCA1 may be written as \"11q1.4-q2.1\", meaning it is on chromosome 11, long arm, somewhere in the range of band 1, sub-band 4, and band 2, sub-band 1.".
- Oculocutaneous_albinism_type_I label "Oculocutaneous albinism type I".
- Oculocutaneous_albinism_type_I sameAs Q1401065.
- Oculocutaneous_albinism_type_I sameAs Okulokutaner_Albinismus_Typ_1.
- Oculocutaneous_albinism_type_I sameAs Albinisme_oculo-cutané_type_I.
- Oculocutaneous_albinism_type_I sameAs m.04gwgkr.
- Oculocutaneous_albinism_type_I sameAs Q1401065.
- Oculocutaneous_albinism_type_I wasDerivedFrom Oculocutaneous_albinism_type_I?oldid=654888067.
- Oculocutaneous_albinism_type_I isPrimaryTopicOf Oculocutaneous_albinism_type_I.
- Oculocutaneous_albinism_type_I name "Oculocutaneous albinism type I".