DNA App Chains | Real-Time Personalization API
App chain |
Chain# |
Description |
Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia |
Chain639 |
This is a rare disease. |
Spinocerebellar Ataxia 6 |
Chain640 |
This is a rare disease. |
Familial Hypercholanemia |
Chain641 |
This is a rare disease. |
Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome |
Chain644 |
This is a rare disease. |
Familial Juvenile Nephronophthisis |
Chain645 |
This is a rare disease. |
Familial Partial Lipodystrophy, Type II |
Chain647 |
This is a rare disease. |
Familial Visceral Amyloidosis |
Chain649 |
This is a rare disease. |
Fanconi Anemia, Complement Group D1 |
Chain650 |
This is a rare disease. |
Fanconi Anemia, Complementation Group A |
Chain651 |
This is a rare disease. |
Fanconi Anemia, Complementation Group C |
Chain652 |
This is a rare disease. |
Fanconi Anemia, Complementation Group D1 |
Chain653 |
This is a rare disease. |
Fanconi Anemia, Complementation Group E |
Chain654 |
This is a rare disease. |
Fanconi Anemia, Complementation Group J |
Chain655 |
This is a rare disease. |
Febrile and afebrile seizures |
Chain656 |
This is a rare disease. |
Fechtner Syndrome |
Chain657 |
This is a rare disease. |
Fibromatosis, juvenile hyaline |
Chain658 |
This is a rare disease. |
Fish-eye Disease |
Chain659 |
This is a rare disease. |
Focal Segmental Glomerulosclerosis |
Chain661 |
This is a rare disease. |
Foveomacular Dystrophy, Adult-onset, with Choroidal Neovascularization |
Chain663 |
This is a rare disease. |
Fragile X Syndrome |
Chain664 |
This is a rare disease. |
Frasier Syndrome |
Chain665 |
This is a rare disease. |
Friedreich Ataxia |
Chain666 |
This is a rare disease. |
Friedreich-Like Ataxia with Isolated Vitamin E Deficiency |
Chain667 |
This is a rare disease. |
Froese Blood Group Antigen |
Chain668 |
This is a rare disease. |
Frontotemporal Dementia |
Chain669 |
This is a rare disease. |
Frontotemporal dementia, with parkinsonism |
Chain670 |
This is a rare disease. |
Frontotemporal Lobar Dementia, Ubiquitin-Positive |
Chain671 |
This is a rare disease. |
Fructosuria |
Chain672 |
This is a rare disease. |
Fuchs Endothelial Corneal Dystrophy |
Chain673 |
This is a rare disease. |
Fucosidosis |
Chain674 |
This is a rare disease. |
Fumarylacetoacetase Pseudodeficiency |
Chain675 |
This is a rare disease. |
Galactosemia |
Chain676 |
This is a rare disease. |
Galactosialidosis |
Chain677 |
This is a rare disease. |
Gangliosidosis GM1 |
Chain678 |
This is a rare disease. |
Gangliosidosis GM1, Adult/Chronic Type |
Chain679 |
This is a rare disease. |