|
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 2
|
13160 |
|
|
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 2; MDDGB2
|
http://purl.obolibrary.org/obo/MONDO_0013160 |
|
|
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B2
|
13160.0 |
|
|
XPNPEP3 nephronophthisis (disease)
|
13163 |
|
|
Parkinson disease 16; PARK16
|
http://purl.obolibrary.org/obo/MONDO_0013167 |
|
|
DFNA39-Dentinogenesis imperfecta 1 syndrome
|
C565316 |
|
|
Alzheimer disease 19 late onset
|
14316 |
|
|
Alzheimer disease 19, late-onset
|
14316 |
|
|
cerebellum astrocytoma (excluding glioblastoma)
|
3165 |
|
|
diencephalon astrocytoma (excluding glioblastoma)
|
3169 |
|
|
Alzheimer disease 19; AD19
|
http://purl.obolibrary.org/obo/MONDO_0014316 |
|
|
nephronophthisis-like nephropathy 1; NPHPL1
|
http://purl.obolibrary.org/obo/MONDO_0013163 |
|
