|
T-B+ SCID due to gamma chain deficiency
|
10315 |
|
|
neonatal brainstem dysfunction
|
15315 |
|
|
familial fibrous dysplasia of the jaws
|
7315 |
|
|
Osebold skeletal dysplasia/osteolysis syndrome
|
11315 |
|
|
congenital muscular dystrophy-FKTN related
|
13156 |
|
|
congenital muscular dystrophy-POMGNT1 related
|
13155 |
|
|
congenital muscular dystrophy-POMT1 related
|
13159 |
|
|
stage 0 endometrium carcinoma
|
3315 |
|
|
systemic lupus erythematosus, susceptibility to, 14
|
13152.0 |
|
|
systemic lupus erythematosus, susceptibility to, 14; SLEB14
|
http://purl.obolibrary.org/obo/MONDO_0013152 |
|
|
congenital Hageman factor deficiency
|
9315 |
|
|
negative rheumatoid factor polyarthritis
|
43152 |
|
|
disseminated nonossifying fibromas in association with cafe-au-lait spots
|
23154 |
|
|
malignant prostate gland neoplasm
|
8315 |
|
