DNA App Chains | Real-Time Personalization API
|
App chain |
Chain# |
Description |
|
Auditory Neuropathy, Temperature-sensitive |
Chain227 |
This is a rare disease. |
|
Autism Spectrum Disorder (Analysis A) |
Chain228 |
This is a rare disease. |
|
Autism Spectrum Disorder (Analysis B) |
Chain229 |
This is a rare disease. |
|
Autism Spectrum Disorder (Analysis C) |
Chain230 |
This is a rare disease. |
|
Asperger Syndrome |
Chain234 |
This is a rare disease. |
|
Mental Retardation |
Chain235 |
This is a rare disease. |
|
Asperger Syndrome |
Chain236 |
This is a rare disease. |
|
Autoimmune and Autoinflammatory Diseases |
Chain237 |
This is a rare disease. |
|
Autoimmune Lymphoproliferative Syndrome, Type IIA |
Chain239 |
This is a rare disease. |
|
Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy |
Chain240 |
This is a rare disease. |
|
Axonal Charcot-Marie-Tooth Disease, Type 2A12 Hereditary Motor and Sensory Neuropathy, Type VI |
Chain241 |
This is a rare disease. |
|
Axonal Charcot-Marie-Tooth Disease, Type 2A2 |
Chain242 |
This is a rare disease. |
|
Axonal Charcot-Marie-Tooth Disease, Type 2D Distal Hereditary Motor Neuropathy, Type V |
Chain243 |
This is a rare disease. |
|
Axonal Charcot-Marie-Tooth Disease, Type 2E |
Chain244 |
This is a rare disease. |
|
Axonal Charcot-Marie-Tooth Disease, Type 2K |
Chain245 |
This is a rare disease. |
|
Axonal Neuropathy with Vocal Cord Paresis |
Chain246 |
This is a rare disease. |
|
Azoospermia, Nonobstructive |
Chain247 |
This is a rare disease. |
|
Bardet-Biedl Syndrome |
Chain248 |
This is a rare disease. |
|
Bardet-Biedl Syndrome 1 |
Chain249 |
This is a rare disease. |
|
Bardet-Biedl Syndrome 13 |
Chain250 |
This is a rare disease. |
|
Bardet-Biedl Syndrome 14 |
Chain251 |
This is a rare disease. |
|
Bardet-Biedl Syndrome 4 |
Chain252 |
This is a rare disease. |
|
Bare Lymphocyte Syndrome, Type I |
Chain253 |
This is a rare disease. |
|
Bart Syndrome |
Chain254 |
This is a rare disease. |
|
Barth Syndrome |
Chain255 |
This is a rare disease. |
|
Barth Syndrome and Noncompaction of the Left Ventricular Myocardium, Familial Isolated |
Chain256 |
This is a rare disease. |
|
Bartter Syndrome |
Chain257 |
This is a rare disease. |
|
Bartter Syndrome, Antenatal, Type 1 |
Chain258 |
This is a rare disease. |
|
Bartter Syndrome, Type 3 |
Chain259 |
This is a rare disease. |
|
Beare-Stevenson Cutis Gyrata Syndrome |
Chain260 |
This is a rare disease. |
|
Benign Familial Hematuria |
Chain261 |
This is a rare disease. |
|
Benign Hereditary Chorea |
Chain262 |
This is a rare disease. |
|
Berardinelli-Seip lipodystrophy |
Chain263 |
This is a rare disease. |
|
Bernard-Soulier Syndrome, Type C |
Chain264 |
This is a rare disease. |
|
Best Macular Dystrophy |
Chain266 |
This is a rare disease. |