DNA App Chains | Real-Time Personalization API
App chain |
Chain# |
Description |
Visual Hallucinations and Hyperphagia with Alzheimer Disease |
Chain1585 |
This is a rare disease. |
Vitamin D Affinity |
Chain1586 |
This is a rare disease. |
Vitamin D-dependent Rickets, Type I |
Chain1587 |
This is a rare disease. |
Vitamin K-Dependent Coagulation Defect |
Chain1588 |
This is a rare disease. |
Vitelliform Macular Dystrophy |
Chain1589 |
This is a rare disease. |
Vohwinkel Syndrome |
Chain1590 |
This is a rare disease. |
Von Hippel-Lindau Syndrome |
Chain1591 |
This is a rare disease. |
Von Willebrand Disease, Type III |
Chain1592 |
This is a rare disease. |
Waardenburg syndrome, Type 3 |
Chain1593 |
This is a rare disease. |
Waardenburg Syndrome, Type IIA |
Chain1594 |
This is a rare disease. |
Waardenburg-Hirschsprung Disease |
Chain1595 |
This is a rare disease. |
Waardenburg-Shah Syndrome |
Chain1596 |
This is a rare disease. |
Waldner Blood Group Antigen |
Chain1597 |
This is a rare disease. |
Walker-Warburg Syndrome |
Chain1598 |
This is a rare disease. |
Warfarin Metabolism |
Chain1599 |
This is a rare disease. |
Weakened Protein Interaction |
Chain1600 |
This is a rare disease. |
Wegener's Granulomatosis |
Chain1601 |
This is a rare disease. |
Werner Syndrome |
Chain1602 |
This is a rare disease. |
Werner Syndrome, Atypical |
Chain1603 |
This is a rare disease. |
WHIM Syndrome |
Chain1604 |
This is a rare disease. |
Wilms Tumor |
Chain1605 |
This is a rare disease. |
Wilson Disease |
Chain1606 |
This is a rare disease. |
Wiskott-Aldrich Syndrome |
Chain1607 |
This is a rare disease. |
Wright Blood Group Antigen |
Chain1610 |
This is a rare disease. |
Xanthinuria, Type I |
Chain1611 |
This is a rare disease. |
Xeroderma Pigmentosum |
Chain1612 |
This is a rare disease. |
Xeroderma Pigmentosum, Complementation Group C |
Chain1613 |
This is a rare disease. |
Xeroderma Pigmentosum, Complementation Group D |
Chain1614 |
This is a rare disease. |
Xeroderma Pigmentosum, Complementation Group E |
Chain1615 |
This is a rare disease. |
Xeroderma Pigmentosum, Complementation Group G |
Chain1616 |
This is a rare disease. |
XRCC3 deficiency |
Chain1617 |
This is a rare disease. |
XY sex reversal and adrenal insufficiency |
Chain1618 |
This is a rare disease. |
XY sex reversal, without adrenal failure |
Chain1619 |
This is a rare disease. |
Zellweger Syndrome |
Chain1620 |
This is a rare disease. |
Zellweger Syndrome, Complementation Group G |
Chain1621 |
This is a rare disease. |