|
CPT1C autosomal dominant pure spastic paraplegia
|
14568 |
|
|
paralytic ileus (disease)
|
4568 |
|
|
spastic paraplegia 73, autosomal dominant
|
14568 |
|
|
spastic paraplegia 73, autosomal dominant; SPG73
|
http://purl.obolibrary.org/obo/MONDO_0014568 |
|
|
autosomal dominant spastic paraplegia 73
|
14568 |
|
|
LARS infantile liver failure
|
24568 |
|
|
Lars infantile liver failure
|
24568 |
|
|
acute infantile liver failure - multisystemic involvement syndrome
|
24568 |
|
|
hereditary spastic paraplegia 73
|
14568 |
|
|
hereditary spastic paraplegia type 73
|
14568 |
|
|
autosomal dominant pure spastic paraplegia caused by mutation in CPT1C
|
14568 |
|
|
infantile liver failure caused by mutation in LARS
|
24568 |
|
