|
nadh-cytochrome b5 reductase deficiency, type ii
|
C537841 |
|
|
hereditary papillary renal carcinoma
|
3789 |
|
|
Hereditary Papillary renal cell cancer
|
3789 |
|
|
hereditary papillary renal cell carcinoma
|
3789 |
|
|
macular dystrophy, retinal, 1, north carolina type
|
C537835 |
|
|
embryonal, 1 rhabdomyosarcoma
|
C537883 |
|
|
lethal neonatal rigidity-multifocal seizure syndrome
|
13784 |
|
|
chromosome 7 ring syndrome
|
C537813 |
|
|
laurence prosser rocker syndrome
|
C537882 |
|
|
X-linked hereditary sensory and autonomic neuropathy with deafness
|
10378 |
|
|
inflammation of serous membrane
|
43786 |
|
|
congenital, with severe central nervous system atrophy and absence of large myelinated fibers muscular dystrophy
|
C563378 |
|
|
dentin dyspalsia, shields type 2
|
D003784 |
|
|
dentin dysplasia, shields type II
|
D003784 |
|
