|
AP4M1 hereditary spastic paraplegia
|
13048 |
|
|
autosomal recessive spastic paraplegia type 61
|
14304 |
|
|
cerebral palsy, spastic quadriplegic, 3, formerly
|
13048 |
|
|
premature chromatid separation trait
|
8304 |
|
|
premature chromatid separation trait; PCS
|
http://purl.obolibrary.org/obo/MONDO_0008304 |
|
|
LDHA glycogen storage disease
|
13047 |
|
|
autosomal recessive spastic paraplegia 50
|
13048 |
|
|
autosomal recessive spastic paraplegia 61
|
14304 |
|
|
hyperphenylalaninemia due to DNAJC12 deficiency
|
44304 |
|
|
mycobacterium tuberculosis, susceptibility to, 3
|
13045.0 |
|
|
Graves disease, susceptibility to, X-linked 1
|
10304 |
|
|
Graves disease, susceptibility to, X-linked 2
|
10304 |
|
|
Graves disease, susceptibility to, X-linked type 1
|
10304 |
|
|
atypical hemolytic-uremic syndrome with B factor anomaly
|
13042 |
|
|
atypical hemolytic-uremic syndrome with C3 anomaly
|
13043 |
|
