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 your 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 v6.x) please enter at least 4 characters:




Results:

Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1
Combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2
EHLERS-DANLOS SYNDROME, NONVASCULAR VARIANT
Ehlers-Danlos syndrome
Ehlers-Danlos syndrome due to tenascin-X deficiency
Ehlers-Danlos syndrome progeroid type
Ehlers-Danlos syndrome type 7A
Ehlers-Danlos syndrome, arthrochalasis type
Ehlers-Danlos syndrome, cardiac valvular type
Ehlers-Danlos syndrome, classic type
Ehlers-Danlos syndrome, classic type, 1
Ehlers-Danlos syndrome, classic type, 2
Ehlers-Danlos syndrome, classic-like, 2
Ehlers-Danlos syndrome, dermatosparaxis type
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type
Ehlers-Danlos syndrome, kyphoscoliotic type 1
Ehlers-Danlos syndrome, musculocontractural type
Ehlers-Danlos syndrome, musculocontractural type 1
Ehlers-Danlos syndrome, musculocontractural type 2
Ehlers-Danlos syndrome, periodontal type 1
Ehlers-Danlos syndrome, periodontal type 2
Ehlers-Danlos syndrome, spondylocheirodysplastic type
Ehlers-Danlos syndrome, spondylodysplastic type, 2
Ehlers-Danlos syndrome, type 3
Ehlers-Danlos syndrome, type 4
Ehlers-danlos syndrome, arthrochalasia type, 2
POLYMICROGYRIA WITHOUT VASCULAR-TYPE EHLERS-DANLOS SYNDROME
Polymicrogyria with or without vascular-type ehlers-danlos syndrome