|
hereditary spastic paraplegia caused by mutation in NIPA1
|
10878 |
|
|
hereditary spastic paraplegia type 6
|
10878 |
|
|
familial spastic paraplegia, autosomal dominant, 3
|
10878 |
|
|
multiple sclerosis, pediatric
|
18784 |
|
|
autosomal dominant osteosclerosis
|
11878 |
|
|
acquired gastric outlet stenosis
|
1878 |
|
|
PROP1 combined pituitary hormone deficiencies, genetic form
|
9878 |
|
|
adult form polyglucosan body disease
|
C564878 |
|
|
ichthyosis mental retardation-epilepsy hypogonadism syndrome
|
C535878 |
|
|
Cytomegalovirus caused retinitis
|
878 |
|
|
adult hypertrophic pyloric stenosis
|
1878 |
|
|
sideroblastic anemia pyridoxine-refractory autosomal recessive
|
8785 |
|
|
anemia, sideroblastic, pyridoxine-refractory, autosomal recessive
|
8785 |
|
|
sideroblastic anemia pyridoxine-responsive autosomal recessive
|
8786 |
|
|
anemia, sideroblastic, pyridoxine-responsive, autosomal recessive
|
8786 |
|
