Gene | Disease |
---|---|
ATXN1 | Spinocerebellar ataxia |
Huntington’s disease | |
ATXN3 | Machado-joseph disease |
Spinocerebellar ataxias | |
ATXN8 | Spinocerebellar Ataxia Type 8 |
BMP2K | Internuclear ophthalmoplegia |
Ulnar neuropathy | |
FOXP2 | Speech-language disorders |
Blepharophimosis | |
Premature ovarian failure | |
Autism | |
Dyslexia | |
HTT | Huntington’s disease |
Spinocerebellar ataxia | |
MAML | Mucoepidermoid carcinoma |
Hidradenoma | |
Lipoadenoma | |
Epithelial-myoepithelial carcinoma | |
MED12 | FG syndrome |
Intellectual disability | |
Schizophrenia | |
MED15 | Epicondylitis |
NCOA3 | Breast cancer |
Ovarian carcinoma | |
PAXIP1 | Spinocerebellar ataxia |
TAF15 | Chondrosarcoma |
Peripheral primitive neuroectodermal tumor | |
Amyotrophic lateral sclerosis | |
Sarcoma | |
Liposarcoma | |
TOX3 | Breast cancer |
TPB | Spinocerebellar ataxia |
Tuberculosis | |
 | Huntington’s disease |