|
multiple mitochondrial dysfunctions syndrome 6
|
54785.0 |
|
|
Prader-Willi syndrome due to translocation
|
15785.0 |
|
|
malignant secondary hypertension
|
1785.0 |
|
|
cleft palate cardiac defect ectrodactyly
|
22785.0 |
|
|
henipavirus infectious disease
|
5785.0 |
|
|
Henoch-Schoenlein purpura
|
6785.0 |
|
|
hereditary spastic paraplegia 19
|
11785.0 |
|
|
obsolete 15q24 microdeletion syndrome
|
19785.0 |
|
|
maternally-inherited diabetes and deafness
|
10785.0 |
|
|
polydactyly, postaxial, type a10
|
32785.0 |
|
