|
Developmental Verbal Dyspraxia |
Chain513 |
This is a rare disease. |
|
Diabetes Insipidus, Central |
Chain514 |
This is a rare disease. |
|
Diabetes Insipidus, Nephrogenic |
Chain515 |
This is a rare disease. |
|
Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans |
Chain516 |
This is a rare disease. |
|
Diabetes, MODY1 |
Chain520 |
This is a rare disease. |
|
Diarrhea, Malabsorptive, Congenital |
Chain522 |
This is a rare disease. |
|
Diastrophic Dysplasia |
Chain523 |
This is a rare disease. |
|
Diego Blood Group Antigen |
Chain524 |
This is a rare disease. |
|
Dihydropteridine Reductase Deficiency |
Chain525 |
This is a rare disease. |
|
Dihydropyrimidine Dehydrogenase Deficiency & Possible 5-FU Toxicity |
Chain67 |
Determine predisposition for DPD deficiency |
|
Dilatative Myopathy |
Chain526 |
This is a rare disease. |
|
Dilated cardiomyopathy |
Chain24 |
Determine the risk of death caused resctrictive cardiomyopathy |
|
Disordered Steroidogenesis Due to POR Deficiency |
Chain527 |
This is a rare disease. |
|
Disseminated Infection with BCG and Salmonella enteritidis |
Chain528 |
This is a rare disease. |
|
Distal Arthrogryposis Syndrome 1 |
Chain529 |
This is a rare disease. |
|
Distal Arthrogryposis Syndrome 2b |
Chain530 |
This is a rare disease. |
|
Distal Myopathy with Anterior Tibial Onset |
Chain1053 |
This is a rare disease. |
|
Distal Myopathy with Decreased Caveolin 3 |
Chain1109 |
This is a rare disease. |
|
Distal Renal Tubular Acidosis |
Chain531 |
This is a rare disease. |
|
Distal Renal Tubular Acidosis with Late-onset Sensorineural Hearing Loss |
Chain532 |
This is a rare disease. |
|
Distal Renal Tubular Acidosis with Progressive Deafness |
Chain533 |
This is a rare disease. |
|
Dombrock Blood Group |
Chain534 |
This is a rare disease. |
|
Dombrock-null Phenotype |
Chain535 |
This is a rare disease. |
|
Dopamine Beta Hydroxylase Deficiency |
Chain536 |
This is a rare disease. |
|
Drug-induced Hemolysis |
Chain70 |
Determine risk of red blood cell dispruption from drugs |
|
Dubin-Johnson Syndrome |
Chain538 |
This is a rare disease. |
|
Dysalbuminemic Hyperthyroxinaemia, Familial |
Chain539 |
This is a rare disease. |
|
Dysautonomia, Familial |
Chain540 |
This is a rare disease. |
|
Dysfibrinogenemia (Analysis A) |
Chain541 |
Fibrinogen Amiens 1 Fibrinogen Amiens 2 Fibrinogen Bergamo 3 Fibrinogen Bern 2 Fibrinogen Bicetre 1 Fibrinogen Birmingham 1 Fibrinogen CHapel Hill 2 Fibrinogen Clermont-Ferrand 1 Fibrinogen Giessen 1 Fibrinogen Leitchfield Fibrinogen |
|
Dysfibrinogenemia (Analysis B) |
Chain542 |
This is a rare disease. |
|
Dysfibrinogenemia (Analysis C) |
Chain543 |
This is a rare disease. |
|
Dysfibrinogenemia (Analysis D) |
Chain544 |
Fibrinogen Bergamo 1 Fibrinogen Hershey 2 Fibrinogen Homburg 2 Fibrinogen Homburg 3 Fibrinogen Kawaguchi 1 Fibrinogen Leogan Fibrinogen Metz 1 Fibrinogen New Albany Fibrinogen Osaka 1 Fibrinogen Schwarzach 1 Fibrinogen Stony Brook 1 Fib |
|
Dystonia 12 |
Chain547 |
This is a rare disease. |
|
Dystonia, Adult-onset |
Chain548 |
This is a rare disease. |
|
Dystonia, Dopa-responsive Dystonia with Motor Delay |
Chain550 |
This is a rare disease. |
