DNA App Chains | Real-Time Personalization API

App chain Chain# Description
Poor Paclitaxel Metabolism Chain1291 This is a rare disease.
Porphyria Cutanea Tarda Chain1292 This is a rare disease.
Porphyria, Acute Hepatic Chain1293 This is a rare disease.
Porphyria, Acute Intermittent Chain1294 This is a rare disease.
Porphyria, Acute Intermittent, Nonerythroid Variant Chain1295 This is a rare disease.
Porphyria, Variegate Chain1296 This is a rare disease.
Possible Association with Cleft Lip, Alveolus, and Palate Chain1297 This is a rare disease.
Possible Association with Crohn's Disease Chain1298 This is a rare disease.
Sarcoidosis, Early-onset Chain1299 This is a rare disease.
Possible association with Higher Plasma TGF-beta Concentration Chain1300 This is a rare disease.
Possible Hearing Impairment Chain1301 This is a rare disease.
Possible Protein Z Deficiency Chain1302 This is a rare disease.
Possible Risk of Total Anomalous Pulmonary Venous Return Chain1303 This is a rare disease.
Ataxia Telangiectasia Chain1305 This is a rare disease.
Possibly associated with Developmental Verbal Dyspraxia Chain1306 This is a rare disease.
Possibly associated with Nonsyndromic Cleft Lip with or without Cleft Palate Chain1307 This is a rare disease.
Possibly associated with Nonsyndromic Sensorineural Deafness Chain1308 This is a rare disease.
Posterior Polymorphons Corneal Dystrophy 1 Chain1309 This is a rare disease.
Prealbumin Chicago Euthyroid Dystransthyretinemic Hyperthyroxinemia Chain1310 This is a rare disease.
Pre-B-Cell Acute Lymphoblastic Leukemia Chain1311 This is a rare disease.
Precocious Puberty, Male-Limited Chain1312 This is a rare disease.
Preeclampsia Chain1313 This is a rare disease.
Preeclampsia/Eclampsia Chain1314 This is a rare disease.
Reduced Plasma Factor VII Levels Chain1364 This is a rare disease.
Primary Congenital Glaucoma Chain1318 This is a rare disease.
Primary Spontaneous Pneumothorax Chain1319 This is a rare disease.
Progressive External Ophthalmoplegia with Hypogonadism Chain1320 This is a rare disease.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions Chain1321 This is a rare disease.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Type 2 Chain1322 This is a rare disease.
Progressive Familial Intrahepatic Cholestasis Chain1323 This is a rare disease.
Benign Recurrent Intrahepatic Cholestasis Chain1324 This is a rare disease.
Progressive Supranuclear Palsy (Analysis A) Chain1325 This is a rare disease.
Progressive Supranuclear Palsy (Analysis B) Chain1326 This is a rare disease.
Parkinson Disease Chain1327 This is a rare disease.
Prolonged Bleeding Time due to Plasminogen Activator Inhibitor 1 Deficiency Chain1328 This is a rare disease.