|
Tunglang savage Bellman syndrome
|
17921 |
|
|
OI, type 9 osteogenesis imperfecta, type 9
|
C564921 |
|
|
congenital factor V deficiency
|
9210 |
|
|
sillence type II-III, without abnormality of type i collagen osteogenesis imperfecta
|
C564921 |
|
|
OI, type IX osteogenesis imperfecta, type IX
|
C564921 |
|
|
glycogenosis Fanconi EXACT
|
9216 |
|
|
Fanconi Anemia, Estren-Dameshek variant
|
9215 |
|
|
Fanconi-Bickel syndrome; FBS
|
http://purl.obolibrary.org/obo/MONDO_0009216 |
|
|
Farber lipogranulomatosis; FRBRL
|
http://purl.obolibrary.org/obo/MONDO_0009218 |
|
|
hereditary Factor V deficiency
|
9210 |
|
|
hereditary factor V deficiency
|
9210 |
|
|
congenital factor VII deficiency
|
9211 |
|
