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.