DNA App Chains | Real-Time Personalization API
App chain |
Chain# |
Description |
Epidermolytic Hyperkeratosis |
Chain596 |
This is a rare disease. |
Nevus, Epidermal, Epidermolytic Hyerkeratotic Type |
Chain597 |
This is a rare disease. |
Epilepsy, Benign Neonatal |
Chain598 |
This is a rare disease. |
Epilepsy, Progressive Myoclonus |
Chain600 |
This is a rare disease. |
Episodic ataxia |
Chain601 |
This is a rare disease. |
Episodic ataxia / myokymia |
Chain602 |
This is a rare disease. |
Episodic Ataxia, Type 2 |
Chain603 |
This is a rare disease. |
Epstein Syndrome |
Chain606 |
This is a rare disease. |
Erythermalgia, primary |
Chain607 |
This is a rare disease. |
Erythrocyte Lactate Transporter Defect |
Chain608 |
This is a rare disease. |
Escobar Syndrome |
Chain609 |
This is a rare disease. |
Estrogen Resistance |
Chain610 |
This is a rare disease. |
Excessive Daytime Sleepiness |
Chain612 |
This is a rare disease. |
Exercise Intolerance |
Chain613 |
This is a rare disease. |
Exostoses, Multiple, Type II |
Chain614 |
This is a rare disease. |
Extrapyramidal Movement Disorder |
Chain615 |
This is a rare disease. |
Fabry Disease |
Chain616 |
This is a rare disease. |
Fabry Disease, Cardiac Variant |
Chain617 |
This is a rare disease. |
Factor V and Factor VIII Deficiency, Combined |
Chain619 |
This is a rare disease. |
Factor VII Deficiency |
Chain620 |
This is a rare disease. |
Factor X Deficiency |
Chain621 |
This is a rare disease. |
Factor XII Deficiency |
Chain622 |
This is a rare disease. |
Fallopian tube cancer |
Chain623 |
This is a rare disease. |
Familial Advanced Sleep Phase Syndrome |
Chain624 |
This is a rare disease. |
Familial Alzheimer Disease 1 |
Chain625 |
This is a rare disease. |
Familial Alzheimer Disease 4 |
Chain626 |
This is a rare disease. |
Familial Cold Autoinflammatory Syndrome 1 |
Chain629 |
This is a rare disease. |
Familial Dysautonomia |
Chain631 |
This is a rare disease. |
Familial Erythrocytosis |
Chain632 |
This is a rare disease. |
Familial Hypercholesterolemia |
Chain642 |
This is a rare disease. |
Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome |
Chain643 |
This is a rare disease. |
Sporadic Hemiplegic Migraine (Analysis C) |
Chain635 |
This is a rare disease. |
Familial Hemiplegic Migraine 2 |
Chain636 |
This is a rare disease. |
Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia |
Chain637 |
This is a rare disease. |
Sporadic Hemiplegic Migraine with Progressive Cerebellar Ataxia |
Chain638 |
This is a rare disease. |