|
chromosome 2p12-p11.2 deletion syndrome
|
13309 |
|
|
congenital estrogen deficiency
|
13301 |
|
|
deafness, autosomal dominant type 51
|
13305 |
|
|
von willebrand's disease 2
|
13304 |
|
|
Noonan syndrome-like disorder with JMML
|
13308 |
|
|
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
|
13308 |
|
|
Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia
|
13308 |
|
|
Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia; NSLL
|
http://purl.obolibrary.org/obo/MONDO_0013308 |
|
|
von Willebrand disease type 2
|
13304 |
|
|
von Willebrand's disease type 2
|
13304 |
|
|
von Willebrand disease type II
|
13304 |
|
|
VON WILLEBRAND disease, type 2
|
13304 |
|
|
Von Willebrand disease, type 2
|
13304 |
|
|
VON WILLEBRAND disease, type 2; VWD2
|
http://purl.obolibrary.org/obo/MONDO_0013304 |
|
