Preferred Name |
VON WILLEBRAND DISEASE, TYPE 1 |
Synonyms |
VWD, TYPE 1 |
ID |
http://purl.bioontology.org/ontology/OMIM/193400 |
altLabel |
VWD, TYPE 1 VON WILLEBRAND DISEASE, TYPE I VWD1 |
cui |
C1264039 |
Gene Locus |
12p13.3 |
Gene Symbol |
VWF F8VWF |
Has manifestation |
http://purl.bioontology.org/ontology/OMIM/MTHU027549 http://purl.bioontology.org/ontology/OMIM/MTHU036809 http://purl.bioontology.org/ontology/OMIM/MTHU009110 http://purl.bioontology.org/ontology/OMIM/MTHU027555 http://purl.bioontology.org/ontology/OMIM/MTHU027553 http://purl.bioontology.org/ontology/OMIM/MTHU027551 http://purl.bioontology.org/ontology/OMIM/MTHU001112 http://purl.bioontology.org/ontology/OMIM/MTHU000449 http://purl.bioontology.org/ontology/OMIM/MTHU000572 http://purl.bioontology.org/ontology/OMIM/MTHU027554 http://purl.bioontology.org/ontology/OMIM/MTHU027552 |
MIMTYPEMEANING |
Phenotype description, molecular basis known. |
notation |
193400 |
OMIM Entry Type |
3 |
OMIM MimType Value |
pound |
prefLabel |
VON WILLEBRAND DISEASE, TYPE 1 |
tui |
T047 |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.bioontology.org/ontology/MESH/D056725 | Medical Subject Headings | CUI | |
http://purl.bioontology.org/ontology/MESH/D056725 | Medical Subject Headings | LOOM |