DNA App Chains | Real-Time Personalization API
App chain |
Chain# |
Description |
Severe Combined Immunodeficiency (SCID), B Cell-negative |
Chain1436 |
This is a rare disease. |
Severe Combined Immunodeficiency (SCID), B Cell-negative Omenn Syndrome |
Chain1437 |
This is a rare disease. |
Severe Combined Immunodeficiency (SCID), T Cell-negative, B Cell-negative, NK Cell-negative |
Chain1438 |
This is a rare disease. |
Severe Combined Immunodeficiency, Athabascan-Type |
Chain1439 |
This is a rare disease. |
Severe Combined Immunodeficiency, T Cell-negative, B Cell-positive, NK Cell-positive |
Chain1440 |
This is a rare disease. |
Superoxide Dismutase, Elevated Extracellular |
Chain1497 |
This is a rare disease. |
Supravalvular Aortic Stenosis |
Chain1498 |
This is a rare disease. |
Severe Language Deficits in Autism |
Chain1443 |
This is a rare disease. |
Increased Rigid-Compulsive Behaviors in Autism |
Chain1444 |
This is a rare disease. |
Autism (Analysis C) |
Chain1445 |
This is a rare disease. |
Severe Metachromatic Leukodystrophy |
Chain1446 |
This is a rare disease. |
Severe Toxicity during Irinotecan Treatment |
Chain1447 |
This is a rare disease. |
Shah-Waardenburg Syndrome |
Chain1448 |
This is a rare disease. |
Short Chain Acyl-CoA-dehydrogenase Deficiency |
Chain1449 |
This is a rare disease. |
Short stature |
Chain1450 |
This is a rare disease. |
Shorter QT Interval |
Chain1451 |
This is a rare disease. |
Sialidosis, Type II |
Chain1452 |
This is a rare disease. |
Tangier Disease |
Chain1510 |
This is a rare disease. |
Sickle Cell Anemia |
Chain1454 |
This is a rare disease. |
Sideroblastic Anemia and Spinocerebellar Ataxia |
Chain1455 |
This is a rare disease. |
Sideroblastic Anemia, Hereditary |
Chain1456 |
This is a rare disease. |
Simpson-Golabi-Behmel Syndrome, Type 1 |
Chain1457 |
This is a rare disease. |
Sinus Node Disease |
Chain1458 |
This is a rare disease. |
Sitosterolemia |
Chain1459 |
This is a rare disease. |
Sjogren-Larsson Syndrome |
Chain1460 |
This is a rare disease. |
Skin cancer, association with |
Chain1461 |
This is a rare disease. |
Slowed Motor and Sensory Nerve Conduction Velocities |
Chain1463 |
This is a rare disease. |
Small Patella Syndrome |
Chain1464 |
This is a rare disease. |
Smith-Lemli-Opitz Syndrome |
Chain1465 |
This is a rare disease. |
Spastic paralysis, infantile-onset |
Chain1466 |
This is a rare disease. |
Spastic paraplegia |
Chain1467 |
This is a rare disease. |
Spastic Paraplegia 10 |
Chain1468 |
This is a rare disease. |
Spastic Paraplegia 3 |
Chain1469 |
This is a rare disease. |
Spastic paraplegia, autosomal dominant |
Chain1470 |
This is a rare disease. |
Blood clot risk |
Chain1527 |
Blood clot risk. |