|
periventricular nodular heterotopia 3
|
11967 |
|
|
familial temporal lobe epilepsy
|
11965 |
|
|
SPG11 amyotrophic lateral sclerosis
|
11196 |
|
|
autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCA
|
11968 |
|
|
autosomal recessive limb-girdle muscular dystrophy type 2D
|
11968 |
|
|
muscular dystrophy, limb-girdle, type 2D
|
11968 |
|
|
muscular dystrophy limb-girdle with alpha-sarcoglycan
|
11968 |
|
|
familial temporal lobe epilepsy 2
|
11965 |
|
|
familial temporal lobe epilepsy type 2
|
11965 |
|
|
schizophrenia susceptibility locus, chromosome 10Q-Related
|
http://purl.obolibrary.org/obo/MONDO_0011960 |
|
|
muscular dystrophy, limb-girdle, type 2D; LGMD2D
|
http://purl.obolibrary.org/obo/MONDO_0011968 |
|
|
schizophrenia susceptibility locus, chromosome 10Q-related
|
11960 |
|
|
hereditary sensory neuropathy type 1B
|
11961 |
|
|
disease by molecular activity disrupted
|
21196.0 |
|
|
hereditary sensory neuropathy type IB
|
11961 |
|
