|
Pulmonary Surfactant Metabolism Dysfunction, Type 2 |
Chain1348 |
This is a rare disease. |
|
Pseudoxanthoma Elasticum |
Chain1347 |
This is a rare disease. |
|
Pseudovaginal Perineoscrotal Hypospadias |
Chain1346 |
This is a rare disease. |
|
Pseudorheumatoid Dysplasia, Progressive |
Chain1345 |
This is a rare disease. |
|
Pseudohypoparathyroidism, Type 1A |
Chain1344 |
This is a rare disease. |
|
Pseudohypoaldosteronism, Type I |
Chain1343 |
This is a rare disease. |
|
Pseudohypoaldosteronism, Type 1 |
Chain1342 |
This is a rare disease. |
|
Pseudohermaphroditism, male |
Chain1341 |
This is a rare disease. |
|
Pseudohermaphroditism |
Chain1340 |
This is a rare disease. |
|
Pseudoachondroplasia |
Chain1338 |
This is a rare disease. |
|
Protoporphyria, Erythropoietic |
Chain1337 |
This is a rare disease. |
|
Protection against Myocardial Infarction |
Chain1336 |
This is a rare disease. |
|
Protection against Major Depression |
Chain964 |
This is a rare disease. |
|
Protection against Autism |
Chain1335 |
This is a rare disease. |
|
Protection against Anxiety Disorders |
Chain963 |
This is a rare disease. |
|
Prostate cancer |
Chain1333 |
This is a rare disease. |
|
Prostate Cancer, Somatic Prostate Cancer, Hereditary |
Chain1334 |
This is a rare disease. |
|
Properdin Deficiency, Type II |
Chain1331 |
This is a rare disease. |
|
Properdin Deficiency, Type I |
Chain1330 |
This is a rare disease. |
|
Promoter Activity |
Chain1329 |
This is a rare disease. |
|
Prolonged Bleeding Time due to Plasminogen Activator Inhibitor 1 Deficiency |
Chain1328 |
This is a rare disease. |
|
Prolactinoma, Hyperparathyroid, Carcinoid Syndrome |
Chain1080 |
This is a rare disease. |
|
Progressive Supranuclear Palsy (Analysis B) |
Chain1326 |
This is a rare disease. |
|
Progressive Supranuclear Palsy (Analysis A) |
Chain1325 |
This is a rare disease. |
|
Progressive Familial Intrahepatic Cholestasis |
Chain1323 |
This is a rare disease. |
|
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Type 2 |
Chain1322 |
This is a rare disease. |
|
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions |
Chain1321 |
This is a rare disease. |
|
Progressive External Ophthalmoplegia with Hypogonadism |
Chain1320 |
This is a rare disease. |
|
Primary Spontaneous Pneumothorax |
Chain1319 |
This is a rare disease. |
|
Primary Pulmonary Hypertension |
Chain95 |
Determine predisposition for pulmonary hypertension |
|
Primary Congenital Glaucoma |
Chain1318 |
This is a rare disease. |
|
Preeclampsia/Eclampsia |
Chain1314 |
This is a rare disease. |
|
Preeclampsia |
Chain1313 |
This is a rare disease. |
|
Predisposed to excel at power-based physical activities and sports |
Chain17 |
Determines predisposition to excelling at power based sports and exercises. |
|
Predisposed to excel at endurance-based physical activities and sports |
Chain18 |
Determines whether person is predisposed to excelling at endurance based sports and exercises. |
