|
paternal monosomy 14q32.2
|
16780 |
|
|
maternal monosomy 14q32.2
|
16781 |
|
|
leukodystrophy, hypomyelinating, 15
|
54782 |
|
|
leukodystrophy, hypomyelinating, 15; HLD15
|
http://purl.obolibrary.org/obo/MONDO_0054782 |
|
|
cone-ROD dystrophy 16; CORD16
|
http://purl.obolibrary.org/obo/MONDO_0013786 |
|
|
spinocerebellar ataxia 17
|
11781 |
|
|
spinocerebellar ataxia 17; SCA17
|
http://purl.obolibrary.org/obo/MONDO_0011781 |
|
|
spastic paraplegia 19, autosomal dominant
|
11785 |
|
|
spastic paraplegia 19, autosomal dominant; SPG19
|
http://purl.obolibrary.org/obo/MONDO_0011785 |
|