|
Unknown
Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
|
| Disease merge term |
Disease name |
Evidence |
References |
Source |
| Mental retardation |
syndromic intellectual disability |
N/A |
N/A |
GenCC |
|
|
Associations from Text Mining
Disease associations identified through Pubtator
|
| Disease Name |
Relationship Type |
References |
| Alcohol Related Disorders |
Associate
|
33482199 |
| Autism Spectrum Disorder |
Associate
|
26576547, 33482199, 37167322, 37572851 |
| Autistic Disorder |
Associate
|
26576547, 37339871 |
| Colorectal Neoplasms |
Associate
|
28105922 |
| Congenital Abnormalities |
Associate
|
26576547 |
| Developmental Disabilities |
Associate
|
32743835, 33628804, 34946857, 37339871 |
| Fibrous Dysplasia Polyostotic |
Associate
|
37339871, 37572851 |
| Fragile X Syndrome |
Associate
|
34946857 |
| Genetic Diseases Inborn |
Associate
|
33628804 |
| Hepatitis C |
Associate
|
35836293 |
| Intellectual Disability |
Associate
|
26168268, 26576547, 33628804, 37167322, 37572851 |
| Megalencephaly |
Associate
|
26576547, 29296277, 33628804, 34946857, 37572851 |
| Mental Disorders |
Associate
|
33628804 |
| Motor Skills Disorders |
Associate
|
37572851 |
| Multiple Sclerosis |
Associate
|
34889895 |
| Muscle Hypotonia |
Associate
|
26576547, 33628804, 37572851 |
| Neoplasms |
Associate
|
34135559 |
| Osteogenesis imperfecta type 2A |
Associate
|
26168268 |
| Parkinson Disease Secondary |
Associate
|
32743835 |
| Psychomotor Disorders |
Associate
|
34946857 |
| Seizures |
Associate
|
26576547, 37572851 |
| Simpson Golabi Behmel syndrome |
Associate
|
25972378 |
| Speech Disorders |
Associate
|
33628804 |
| Stomach Neoplasms |
Associate
|
34135559 |
| Syndrome |
Associate
|
37339871 |
|