myopathies, tubular aggregate
|
D020914 |
|
intellectual disability, autosomal dominant 49
|
30914 |
|
mental retardation, autosomal dominant 49
|
30914 |
|
mental retardation, autosomal dominant 49; MRD49
|
http://purl.obolibrary.org/obo/MONDO_0030914 |
|
hypotrichosis-lymphedema-telangiectasia syndrome; HLTS
|
http://purl.obolibrary.org/obo/MONDO_0011914 |
|
pediatric brainstem cancer
|
2914 |
|
myopathies, x-linked centronuclear
|
D020914 |
|
acute intoxication by Blighia sapida
|
19140 |
|
cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1
|
914 |
|
cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1; CADASIL1
|
http://purl.obolibrary.org/obo/MONDO_0000914 |
|
myopathy, x-linked centronuclear
|
D020914 |
|
x linked centronuclear myopathy
|
D020914 |
|
autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
|
914 |
|
dystonic disorder caused by mutation in HPCA
|
9141 |
|
Sanchez Cascos cardioauditory syndrome
|
8914 |
|