DNA App Chains | Real-Time Personalization API
App chain |
Chain# |
Description |
Meckel Syndrome, Type 1 |
Chain1003 |
This is a rare disease. |
Meckel Syndrome, Type 3 |
Chain1004 |
This is a rare disease. |
Meckel Syndrome, Type 4 |
Chain1005 |
This is a rare disease. |
Mediterranean Macrothrombocytopenia |
Chain1006 |
This is a rare disease. |
Bernard-Soulier Syndrome, Type A |
Chain1007 |
This is a rare disease. |
Medulloblastoma |
Chain1008 |
This is a rare disease. |
Meesmann Corneal Dystrophy |
Chain1009 |
This is a rare disease. |
Megablastic Anemia, Norwegian |
Chain1010 |
This is a rare disease. |
Megalencephalic Leukoencephalopathy with Subcortical Cysts |
Chain1011 |
This is a rare disease. |
Megaloblastic Anemia, Finnish Type |
Chain1012 |
This is a rare disease. |
Megaloblastic Anemia, Thiamine-Responsive |
Chain1013 |
This is a rare disease. |
Melas Syndrome |
Chain1014 |
This is a rare disease. |
Melnick-Needles syndrome |
Chain1015 |
This is a rare disease. |
Meningioma |
Chain1016 |
This is a rare disease. |
Li-Fraumeni Syndrome |
Chain1017 |
This is a rare disease. |
Menkes Disease |
Chain1018 |
This is a rare disease. |
Menorrhagia |
Chain1019 |
This is a rare disease. |
Mental Retardation |
Chain1020 |
This is a rare disease. |
Mental Retardation with Retinitis Pigmentosa |
Chain1021 |
This is a rare disease. |
Mental Retardation, Nonsyndromic |
Chain1022 |
This is a rare disease. |
Mental Retardation, X-linked 19 |
Chain1023 |
This is a rare disease. |
Mental Retardation, X-linked, Syndromic 10 |
Chain1024 |
This is a rare disease. |
Mental Retardation-hypotonic Facies Syndrome |
Chain1025 |
This is a rare disease. |
MERRF Syndrome |
Chain1026 |
This is a rare disease. |
MERRF/MELAS Overlap Syndrome |
Chain1027 |
This is a rare disease. |
Metabolic Syndrome |
Chain1028 |
This is a rare disease. |
Hyperapobetalipoproteinemia |
Chain1029 |
This is a rare disease. |
Methionine synthase reductase deficiency |
Chain1030 |
This is a rare disease. |
Methylmalonic Aciduria and Homocystinuria, cblC Type |
Chain1031 |
This is a rare disease. |
Methylmalonic Aciduria, cblB type |
Chain1032 |
This is a rare disease. |
Methylmalonic Aciduria, mut(0) Type |
Chain1033 |
This is a rare disease. |
Microhaematuria and protinuria |
Chain1034 |
This is a rare disease. |
Migraine |
Chain1037 |
This is a rare disease. |
Mild Pelizaeus-Merzbacher Disease |
Chain1038 |
This is a rare disease. |
Mild, Cutaneous-only Congenital Erythropoietic Porphyria |
Chain1039 |
This is a rare disease. |