|
muscular dystrophy-dystroglycanopathy (limb-girdle) type C 2
|
13162 |
|
|
Parkinson disease 16; PARK16
|
http://purl.obolibrary.org/obo/MONDO_0013167 |
|
|
nephronophthisis-like nephropathy 1; NPHPL1
|
http://purl.obolibrary.org/obo/MONDO_0013163 |
|
|
muscular dystrophy-dystroglycanopathy (limb-girdle) type C3
|
13161 |
|
|
muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2
|
13162 |
|
|
muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2; MDDGC2
|
http://purl.obolibrary.org/obo/MONDO_0013162 |
|
|
muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3
|
13161 |
|
|
muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3; MDDGC3
|
http://purl.obolibrary.org/obo/MONDO_0013161 |
|
|
spastic paraplegia 45, autosomal recessive
|
13165 |
|
|
cardiomyopathy, dilated, 1DD
|
13168 |
|
|
dilated cardiomyopathy 1DD
|
13168 |
|
|
cardiomyopathy, dilated, 1DD; CMD1DD
|
http://purl.obolibrary.org/obo/MONDO_0013168 |
|
|
spastic paraplegia 45, autosomal recessive; SPG45
|
http://purl.obolibrary.org/obo/MONDO_0013165 |
|
|
4 alpha aminobutyrate transaminase deficiency
|
13166 |
|
