|
rare genetic hypothalamic or pituitary disease
|
15968.0 |
|
|
shoulder impingement syndrome
|
6968.0 |
|
|
obsolete 46 XY gonadal dysgenesis
|
1968.0 |
|
|
partial duplication of chromosome 12
|
42968.0 |
|
|
obsolete Osgood-Schlatter disease
|
19968.0 |
|
|
obsolete acute myelomonocytic leukemia
|
4968.0 |
|
|
cholestasis with gallstone, ataxia, and visual disturbance
|
8968.0 |
|
|
autosomal recessive limb-girdle muscular dystrophy type 2D
|
11968.0 |
|
|
renal tubular acidosis, distal, 2, with progressive sensorineural hearing loss
|
9968.0 |
|
|
melanoma tumor antigen Gp90
|
7968.0 |
|
|
encephalopathy, progressive, with amyotrophy and optic atrophy
|
14968.0 |
|
