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Online Mendelian Inheritance in Man
Last uploaded:
August 28, 2024
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Preferred Name | GLYCOPROTEIN Ib, PLATELET, ALPHA POLYPEPTIDE | |
Synonyms |
GLYCOCALICIN GP1BA CD42B BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO GP Ib, ALPHA SUBUNIT BERNARD-SOULIER SYNDROME, TYPE A1 PLATELET GLYCOPROTEIN Ib, ALPHA POLYPEPTIDE PLATELET GLYCOPROTEIN Ib POLYMORPHISM VON WILLEBRAND DISEASE, PLATELET-TYPE |
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ID |
http://purl.bioontology.org/ontology/OMIM/606672 |
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altLabel |
GLYCOCALICIN GP1BA CD42B BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO GP Ib, ALPHA SUBUNIT BERNARD-SOULIER SYNDROME, TYPE A1 PLATELET GLYCOPROTEIN Ib, ALPHA POLYPEPTIDE PLATELET GLYCOPROTEIN Ib POLYMORPHISM VON WILLEBRAND DISEASE, PLATELET-TYPE
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cui |
C4016977 C1415186 C3278148 C1280798 C1847711 C3277076
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Gene Locus |
17pter-p12
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Gene Symbol |
BDPLT1 BDPLT3 GP1BA VWDP BSS
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Has allelic variant |
http://purl.bioontology.org/ontology/OMIM/606672.0006 http://purl.bioontology.org/ontology/OMIM/606672.0005 http://purl.bioontology.org/ontology/OMIM/606672.0003 http://purl.bioontology.org/ontology/OMIM/606672.0002 http://purl.bioontology.org/ontology/OMIM/606672.0004 |
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MIMTYPEMEANING |
Gene with known sequence
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notation |
606672
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OMIM Entry Type |
1
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OMIM MimType Value |
star
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prefLabel |
GLYCOPROTEIN Ib, PLATELET, ALPHA POLYPEPTIDE
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tui |
T047 T033 T028
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