|
autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMGNT1
|
13161 |
|
|
autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMT2
|
13162 |
|
|
autosomal recessive limb-girdle muscular dystrophy type 2N
|
13162 |
|
|
autosomal recessive limb-girdle muscular dystrophy type 2O
|
13161 |
|
|
muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT1-Related
|
http://purl.obolibrary.org/obo/MONDO_0013161 |
|
|
muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT1-related
|
13161 |
|
|
muscular dystrophy-dystroglycanopathy, limb-girdle, Pomt2-Related
|
http://purl.obolibrary.org/obo/MONDO_0013162 |
|
|
muscular dystrophy-dystroglycanopathy, limb-girdle, Pomt2-related
|
13162 |
|
|
muscular dystrophy, limb-girdle, type 2N
|
13162 |
|
|
muscular dystrophy, limb-girdle, type 2O
|
13161 |
|
|
osteosclerotic chondrodysplasia, lethal, with intracellular inclusions
|
11316 |
|
|
acute myelomonocytic leukemia
|
20316 |
|
|
Streptococcus infectious meningitis
|
1316 |
|
|
chromosome 2, monosomy 2q24
|
C538316 |
|
|
chronic recurrent multifocal osteomyelitis, congenital
|
12316 |
|
