Reports generated by Genomapp’s app are the result of crossing our database with your raw data file. If you don’t find a condition in your Genomapp results is because you don’t have a marker related to that condition in your raw data file or if it exists in you file, it is not in our database.

Examples of conditions included in our database: Alzheimer‘s, Parkinson‘s, Ehlers-Danlos, cancer.

You can also check for particular genes (like BRCA1/BRCA2, PTEN, TP53) and marker numbers (rs80224560, rs121913630, rs80357336, etc).

To check if a condition is included in our database (Genomapp v5.x) please enter at least 4 characters:


Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome
Parkinson Disease, Juvenile
Parkinson disease
Parkinson disease 1
Parkinson disease 11
Parkinson disease 14
Parkinson disease 15
Parkinson disease 17
Parkinson disease 18
Parkinson disease 19a, juvenile-onset
Parkinson disease 19b, early-onset
Parkinson disease 2
Parkinson disease 20, early-onset
Parkinson disease 21
Parkinson disease 22, autosomal dominant
Parkinson disease 23, autosomal recessive early-onset
Parkinson disease 5
Parkinson disease 6, autosomal recessive early-onset
Parkinson disease 7
Parkinson disease 8, autosomal dominant
Parkinson disease 9
Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1
Parkinson disease, late-onset
Parkinson disease, mitochondrial
Parkinson disease, resistance to
Parkinson-dementia syndrome
Parkinsonism with spasticity, X-linked
Parkinsonism, early onset with mental retardation
Parkinsonism-dystonia, infantile, 1
Parkinsonism-dystonia, infantile, 2
Susceptibility to Parkinson's Disease
Wolff-Parkinson-White pattern
Wolff-Parkinson-White syndrome
Wolff-Parkinson-White syndrome, childhood-onset
X-linked dominant Parkinson's disease
Young-onset Parkinson disease