|
nevus, spindle cell and epithelioid
|
D018332 |
|
|
multiple acyl-CoA dehydrogenase deficiency, severe neonatal type
|
18332 |
|
|
pseudo-von Willebrand disease type 2B
|
8332 |
|
|
Von Willebrand disease, Platelet-type
|
8332 |
|
|
Von Willebrand disease, platelet type
|
8332 |
|
|
pseudo-VON WILLEBRAND disease; VWDP
|
http://purl.obolibrary.org/obo/MONDO_0008332 |
|
|
platelet-type bleeding disorder 3
|
8332 |
|
|
severe acrofrontofacionasal dysostosis
|
C538332 |
|
|
MADD, severe neonatal type
|
18332 |
|
|
glutaric aciduria type 2, severe neonatal type
|
18332 |
|
|
MAD deficiency, severe neonatal type
|
18332 |
|
|
hypospadias, and polysyndactyly syndrome hypertelorism
|
C538332 |
|
|
epithelioid and spindle cell nevus
|
D018332 |
|
