|
hereditary spastic paraplegia 50
|
13048 |
|
|
hereditary spastic paraplegia caused by mutation in AP4M1
|
13048 |
|
|
hereditary spastic paraplegia type 50
|
13048 |
|
|
central auditory pathway disorders
|
D001304 |
|
|
AP4M1 hereditary spastic paraplegia
|
13048 |
|
|
cerebral palsy, spastic quadriplegic, 3, formerly
|
13048 |
|
|
LDHA glycogen storage disease
|
13047 |
|
|
autosomal recessive spastic paraplegia 50
|
13048 |
|
|
atypical hemolytic-uremic syndrome with B factor anomaly
|
13042 |
|
|
mycobacterium tuberculosis, susceptibility to, 3
|
13045.0 |
|
|
atypical hemolytic-uremic syndrome with C3 anomaly
|
13043 |
|
|
atypical hemolytic-uremic syndrome with I factor anomaly
|
13041 |
|
|
atypical hemolytic-uremic syndrome with MCP/CD46 anomaly
|
13040 |
|
|
atypical hemolytic-uremic syndrome with thrombomodulin anomaly
|
13044 |
|
|
hemolytic uremic syndrome, atypical, susceptibility to, 2
|
13040 |
|
