C1832669 |
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) |
DO |
hereditary spastic paraplegia 9A
|
0110824 |
C1832669 |
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) |
MONDO |
hereditary spastic paraplegia 9A
|
0011006 |
C1832669 |
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) |
MSH |
Spastic paraplegia 9, autosomal dominant
|
C536868 |
C1832669 |
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) |
OMIM |
SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT
|
601162 |
C1832669 |
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) |
OMIM |
SPG9A
|
601162 |
C1832669 |
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) |
ORDO |
Autosomal dominant spastic paraplegia type 9A
|
447753 |