DNA App Chains | Real-Time Personalization API
App chain |
Chain# |
Description |
CPT1A Deficiency |
Chain428 |
This is a rare disease. |
CPT2 Deficiency |
Chain429 |
This is a rare disease. |
CPT2 Deficiency, inducable with anesthesia |
Chain430 |
This is a rare disease. |
Craniofrontonasal Syndrome |
Chain431 |
This is a rare disease. |
Craniometaphyseal Dysplasia |
Chain432 |
This is a rare disease. |
Craniosynostosis |
Chain433 |
This is a rare disease. |
Muenke Syndrome |
Chain434 |
This is a rare disease. |
Creutzfeldt-Jakob Syndrome |
Chain435 |
This is a rare disease. |
Crigler-Najjar Syndrome, Type 1 |
Chain437 |
This is a rare disease. |
Crigler-Najjar Syndrome, Type 2 |
Chain438 |
This is a rare disease. |
Crigler-Najjar Syndrome, Type 1 |
Chain439 |
This is a rare disease. |
Gilbert Syndrome |
Chain440 |
This is a rare disease. |
Crouzon syndrome |
Chain446 |
This is a rare disease. |
Crouzon Syndrome with Acanthosis Nigricans Crouzonodermoskeletal Syndrome |
Chain447 |
This is a rare disease. |
Cryptorchidism |
Chain448 |
This is a rare disease. |
Cystathioninuria |
Chain449 |
This is a rare disease. |
Cystic Fibrosis |
Chain450 |
This is a rare disease. |
Cystinuria, non-type I |
Chain453 |
This is a rare disease. |
Cystinuria |
Chain452 |
This is a rare disease. |
Deafness |
Chain457 |
This is a rare disease. |
Danon Disease |
Chain455 |
This is a rare disease. |
Darier Disease |
Chain456 |
This is a rare disease. |
Deafness, Autosomal Dominant 12 |
Chain458 |
This is a rare disease. |
Deafness, Autosomal Dominant 6 |
Chain459 |
This is a rare disease. |
Deafness, Autosomal Recessive 1 |
Chain460 |
This is a rare disease. |
Deafness, Childhood-onset Neurosensory |
Chain461 |
This is a rare disease. |
Deafness, Childhood-onset Neurosensory |
Chain462 |
This is a rare disease. |
Deafness, Congenital Neurosensory |
Chain463 |
This is a rare disease. |
Deafness, Neurosensory |
Chain467 |
This is a rare disease. |
Deafness, Congenital Neurosensory |
Chain465 |
This is a rare disease. |
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia |
Chain466 |
This is a rare disease. |
Deafness, Neurosensory 21 |
Chain468 |
This is a rare disease. |
Deafness, Neurosensory without Vestibular Involvement |
Chain469 |
This is a rare disease. |
Deafness, Nonsyndromic |
Chain470 |
This is a rare disease. |
Deafness, Nonsyndromic Sensorineural |
Chain472 |
This is a rare disease. |