|
hereditary folate malabsorption
|
9238.0 |
|
|
hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase
|
9408.0 |
|
|
dilated cardiomyopathy 2B
|
13848.0 |
|
|
obsolete Japanese encephalitis
|
5816.0 |
|
|
digital dermatitis in cattle
|
25030.0 |
|
|
mitochondrial complex 1 deficiency, nuclear type 15
|
32620.0 |
|
|
postcholecystectomy syndrome
|
6916.0 |
|
|
enlarged vestibular aqueduct syndrome
|
23069.0 |
|
|
partial duplication of the long arm of chromosome 2
|
16953.0 |
|
|
maternal 14q32.2 hypermethylation syndrome
|
16783.0 |
|
|
colorectal cancer, hereditary nonpolyposis, type 2
|
12249.0 |
|
