|
spinocerebellar ataxia, autosomal recessive 24
|
14934.0 |
|
|
leukemia, chronic lymphocytic, susceptibility to, 3
|
12934.0 |
|
|
combined immunodeficiency due to STK4 deficiency
|
13934.0 |
|
|
benign concentric annular macular dystrophy
|
7934.0 |
|
|
genitourinary and/or brain malformation syndrome
|
32934.0 |
|
|
obsolete mucopolysaccharidosis type 1
|
18934.0 |
|
|
intravascular angioleiomyoma
|
2934.0 |
|
|
partial duplication of chromosome 16
|
16934.0 |
|
|
obsolete primary hypertrophic osteoarthropathy
|
1934.0 |
|
|
non-syndromic urogenital tract malformation of male and female
|
15934.0 |
|
|
aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome
|
17934.0 |
|
