|
spastic paraplegia 19, autosomal dominant
|
11785 |
|
|
spastic paraplegia 19, autosomal dominant; SPG19
|
http://purl.obolibrary.org/obo/MONDO_0011785 |
|
|
Moyamoya disease 2; MYMY2
|
http://purl.obolibrary.org/obo/MONDO_0011784 |
|
|
Huntington disease-like 4
|
11781 |
|
|
infantile convulsions and choreoathetosis
|
11178 |
|
|
infantile convulsions and paroxysmal choreoathetosis, familial
|
11178 |
|
|
multiple congenital anomalies syndrome with cloverleaf skull
|
11788 |
|
|
Moyamoya disease caused by mutation in RNF213
|
11784 |
|
|
cloverleaf skull-multiple congenital anomalies syndrome
|
11788 |
|
|
mannosyltransferase 8 deficiency
|
11783 |
|
|
paroxysmal kinesigenic dyskinesia and infantile convulsions
|
11178 |
|
|
paroxysmal kinesigenic dyskinesia with infantile convulsions
|
11178 |
|
