|
early onset autosomal recessive inflammatory bowel disease 28
|
13153 |
|
|
obsolete adenosquamous carcinoma
|
3156.0 |
|
|
X-linked severe combined immunodeficiency
|
10315 |
|
|
retinitis pigmentosa caused by mutation in PDE6G
|
13315 |
|
|
T-B+ severe combined immunodeficiency due to gamma chain deficiency
|
10315 |
|
|
T-B+ severe combined immunodeficiency, X-linked
|
10315 |
|
|
fibula aplasia complex brachydactyly
|
23155 |
|
|
choroidal dystrophy, central areolar, 3
|
13151 |
|
|
choroidal dystrophy, central areolar, 3; CACD3
|
http://purl.obolibrary.org/obo/MONDO_0013151 |
|
|
choroidal dystrophy, central areolar, with or without drusen
|
13151 |
|
|
Hageman Factor deficiency
|
9315 |
|
|
familial multilocular cystic disease of the jaws
|
7315 |
|
