|
SEVERE COMBINED IMMUNODEFICIENCY WITH MICROCEPHALY, GROWTH RETARDATION, AND SENSITIVITY TO IONIZING RADIATION
|
DISO:OMIM |
|
|
SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION DUE TO NHEJ1 DEFICIENCY
|
DISO:OMIM |
|
|
Diabetic peripheral neuropathy in long-standing cases
|
DISO:OMIM |
|
|
Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of
|
DISO:MSH |
|
|
MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY
|
DISO:OMIM |
|
|
ACYL-CoA DEHYDROGENASE 9 DEFICIENCY
|
DISO:OMIM |
|
|
MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY
|
DISO:OMIM |
|
|
PROSTATE CANCER, HEREDITARY, 10
|
DISO:OMIM |
|
|
Prostate Cancer, Hereditary, 10
|
DISO:MSH |
|
