|
deafness, autosomal dominant type 51
|
13305 |
|
|
pseudohermaphroditism, female, due to placental aromatase deficiency
|
13301 |
|
|
chromosome 9q21.11 duplication syndrome
|
13305 |
|
|
commissural cleft, isolated
|
13300 |
|
|
transverse cleft, isolated
|
13300 |
|
|
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 |
|
|
deafness, autosomal dominant 51
|
13305 |
|
|
deafness, autosomal dominant 51; DFNA51
|
http://purl.obolibrary.org/obo/MONDO_0013305 |
|
|
Cbl mutation-associated syndrome
|
13308 |
|
|
autosomal dominant nonsyndromic deafness 51
|
13305 |
|
|
autosomal dominant nonsyndromic deafness type 51
|
13305 |
|
