|
choroidal dystrophy, central areolar, with or without drusen
|
13151 |
|
|
early onset autosomal recessive inflammatory bowel disease 28
|
13153 |
|
|
muscular dystrophy, congenital, Fktn-related
|
13156 |
|
|
muscular dystrophy, congenital, POMGNT1-Related
|
http://purl.obolibrary.org/obo/MONDO_0013155 |
|
|
muscular dystrophy, congenital, POMGNT1-related
|
13155 |
|
|
muscular dystrophy, congenital, Pomt1-Related
|
http://purl.obolibrary.org/obo/MONDO_0013159 |
|
|
muscular dystrophy, congenital, Pomt1-related
|
13159 |
|
|
inflammatory bowel disease 28
|
13153 |
|
|
inflammatory bowel disease type 28
|
13153 |
|
|
inflammatory bowel disease 28, autosomal recessive
|
13153 |
|
|
inflammatory bowel disease 28, autosomal recessive; IBD28
|
http://purl.obolibrary.org/obo/MONDO_0013153 |
|
|
inflammatory bowel disease caused by mutation in IL10RA
|
13153 |
|
|
systemic lupus erythematosus, susceptibility to, 14
|
13152.0 |
|
|
Osebold skeletal dysplasia/osteolysis syndrome
|
11315 |
|
|
congenital muscular dystrophy-FKTN related
|
13156 |
|
