|
autosomal recessive ataxia due to coenzyme Q10 deficiency
|
12784 |
|
|
autosomal recessive ataxia due to ubiquinone deficiency
|
12784 |
|
|
spastic ataxia, autosomal dominant
|
17846 |
|
|
spastic ataxia, autosomal recessive
|
17847 |
|
|
spinocerebellar ataxia, autosomal recessive 9
|
12784 |
|
|
NADH cytochrome b5 reductase deficiency
|
C537841 |
|
|
myopathy, myofibrillar, bag3-related
|
C567843 |
|
|
laurence moon biedl syndrome
|
D007849 |
|
|
skin of body hypersensitivity reaction type II disease
|
17841 |
|
|
dental pulp calcifications
|
D003784 |
|
|
EBV-associated gastric carcinoma
|
17784 |
|
|
nasal cavity carcinoma in situ
|
3784 |
|
|
stage 0 carcinoma of nasal cavity
|
3784 |
|
|
stage 0 carcinoma of the nasal cavity
|
3784 |
|
|
growth retardation, cataract, hearing loss, and unusual appearance microcephaly
|
C567849 |
|
