|
deficiencies, cytochrome oxidase
|
D030401 |
|
|
deficiency, Cytochrome-c oxidase
|
D030401 |
|
|
deficiency, cytochrome oxidase
|
D030401 |
|
|
cytochrome c oxidase deficiency
|
D030401 |
|
|
benign hypertensive renal disease
|
1304 |
|
|
hereditary spastic paraplegia 50
|
13048 |
|
|
hereditary spastic paraplegia 61
|
14304 |
|
|
hereditary spastic paraplegia caused by mutation in AP4M1
|
13048 |
|
|
hereditary spastic paraplegia type 50
|
13048 |
|
|
hereditary spastic paraplegia type 61
|
14304 |
|
|
central auditory pathway disorders
|
D001304 |
|
|
rare skin photosensitivity
|
http://purl.obolibrary.org/obo/MONDO_0019304 |
|
|
ARL6IP1 autosomal recessive complex spastic paraplegia
|
14304 |
|
|
autosomal recessive spastic paraplegia type 61
|
14304 |
|
|
esthesioneuroblastoma, paranasal sinus nasal cavity
|
D018304 |
|
