DNA App Chains | Real-Time Personalization API
|
App chain |
Chain# |
Description |
|
Aarskog-Scott syndrome |
Chain108 |
This is a rare disease. |
|
Aarskog-Scott syndrome with Attention Deficit Hyperactivity Disorder |
Chain109 |
This is a rare disease. |
|
ACADM Deficiency |
Chain110 |
This is a rare disease. |
|
Achromatopsia |
Chain111 |
This is a rare disease. |
|
Achromatopsia 3 |
Chain112 |
This is a rare disease. |
|
Acromesomelic Dysplasia, Maroteaux Type |
Chain113 |
This is a rare disease. |
|
Actin myopathy |
Chain114 |
This is a rare disease. |
|
Acute Hepatic Porphyria, Severe Infantile-onset |
Chain115 |
This is a rare disease. |
|
Acute lymphoblastic leukaemia |
Chain116 |
This is a rare disease. |
|
Acute Lymphoblastic Leukemia |
Chain117 |
This is a rare disease. |
|
Acute Myeloid Leukemia with Complex Karyotype |
Chain118 |
This is a rare disease. |
|
Adenine Phosphoribosyltransferase Deficiency |
Chain119 |
This is a rare disease. |
|
Adenomatous polyposis coli |
Chain120 |
This is a rare disease. |
|
Possible increased risk of adenomatous polyposis coli |
Chain121 |
This is a rare disease. |
|
Adenosine Deaminase Deficiency, Partial |
Chain122 |
This is a rare disease. |
|
Adenosine Monophosphate Deaminase Deficiency |
Chain123 |
This is a rare disease. |
|
Adiponectin Deficiency |
Chain124 |
This is a rare disease. |
|
Adrenal hyperplasia |
Chain125 |
This is a rare disease. |
|
Adrenal Hypoplasia, Congenital |
Chain126 |
This is a rare disease. |
|
Adrenal Insufficiency, Congenital |
Chain127 |
This is a rare disease. |
|
Adrenocortical Tumor |
Chain128 |
This is a rare disease. |
|
Adrenoleukodystrophy, Autosomal Neonatal Form |
Chain129 |
This is a rare disease. |
|
ADSL Deficiency |
Chain130 |
This is a rare disease. |
|
Adult Metachromatic Leukodystrophy |
Chain131 |
This is a rare disease. |
|
Agammaglobulinemia |
Chain132 |
This is a rare disease. |
|
Agammaglobulinemia and Isolated Growth Hormone Deficiency |
Chain133 |
This is a rare disease. |
|
Alagille Syndrome 2 |
Chain134 |
This is a rare disease. |
|
Albinism, Ocular, Type I |
Chain135 |
This is a rare disease. |
|
Albinism, Oculocutaneous, Type III |
Chain136 |
This is a rare disease. |
|
Albumin Variant |
Chain137 |
This is a rare disease. |
|
Alexander Disease |
Chain138 |
This is a rare disease. |
|
Alkaptonuria |
Chain139 |
This is a rare disease. |
|
Allan-Herndon-Dudley Syndrome |
Chain140 |
This is a rare disease. |
|
Allopurinol-induced Severe Cutaneous Adverse Reactions |
Chain141 |
This is a rare disease. |
|
Alopecia Universalis Congenita |
Chain143 |
This is a rare disease. |