| C4721916 |
HMSN Type V |
DO |
Charcot-Marie-Tooth disease type 5
|
0080067 |
| C4721916 |
HMSN Type V |
DO |
hereditary spastic paraplegia
|
2476 |
| C4721916 |
HMSN Type V |
MONDO |
Charcot-Marie-Tooth disease type 5
|
0010877 |
| C4721916 |
HMSN Type V |
MSH |
Spastic Paraplegia, Hereditary
|
D015419 |
| C4721916 |
HMSN Type V |
MSH |
Hereditary Autosomal Dominant Spastic Paraplegia
|
D015419 |
| C4721916 |
HMSN Type V |
MSH |
Autosomal Recessive Hereditary Spastic Paraplegia
|
D015419 |
| C4721916 |
HMSN Type V |
MSH |
Hereditary X-Linked Recessive Spastic Paraplegia
|
D015419 |
| C4721916 |
HMSN Type V |
MSH |
X-Linked, Spastic Paraplegia, Hereditary
|
D015419 |
| C4721916 |
HMSN Type V |
MSH |
HMSN Type V
|
D015419 |
| C4721916 |
HMSN Type V |
OMIM |
PERONEAL MUSCULAR ATROPHY WITH PYRAMIDAL FEATURES, AUTOSOMAL DOMINANT
|
600361 |
| C4721916 |
HMSN Type V |
OMIM |
HEREDITARY MOTOR AND SENSORY NEUROPATHY V
|
600361 |
| C4721916 |
HMSN Type V |
OMIM |
HMSN V
|
600361 |
| C4721916 |
HMSN Type V |
ORDO |
Hereditary motor and sensory neuropathy type 5
|
64751 |