|
Precocious Puberty, Male-Limited |
Chain1312 |
This is a rare disease. |
|
Prealbumin Chicago Euthyroid Dystransthyretinemic Hyperthyroxinemia |
Chain1310 |
This is a rare disease. |
|
Pre-B-Cell Acute Lymphoblastic Leukemia |
Chain1311 |
This is a rare disease. |
|
Posttransfusion Purpura |
Chain1131 |
This is a rare disease. |
|
Posterior Polymorphons Corneal Dystrophy 1 |
Chain1309 |
This is a rare disease. |
|
Postanesthetic apnea risk with succinylcholine, mivacurium, and suxamethonium |
Chain101 |
Determine risk of adverse reactions from medications |
|
Possibly associated with pancreatic cancer |
Chain1241 |
This is a rare disease. |
|
Possibly associated with obesity |
Chain1194 |
This is a rare disease. |
|
Possibly associated with Nonsyndromic Sensorineural Deafness |
Chain1308 |
This is a rare disease. |
|
Possibly associated with Nonsyndromic Cleft Lip with or without Cleft Palate |
Chain1307 |
This is a rare disease. |
|
Possibly associated with Developmental Verbal Dyspraxia |
Chain1306 |
This is a rare disease. |
|
Possible increased risk of adenomatous polyposis coli |
Chain121 |
This is a rare disease. |
|
Possible association with Higher Plasma TGF-beta Concentration |
Chain1300 |
This is a rare disease. |
|
Possible Risk of Total Anomalous Pulmonary Venous Return |
Chain1303 |
This is a rare disease. |
|
Possible Protein Z Deficiency |
Chain1302 |
This is a rare disease. |
|
Possible Hearing Impairment |
Chain1301 |
This is a rare disease. |
|
Possible Association with Crohn's Disease |
Chain1298 |
This is a rare disease. |
|
Possible Association with Cleft Lip, Alveolus, and Palate |
Chain1297 |
This is a rare disease. |
|
Porphyria, Variegate |
Chain1296 |
This is a rare disease. |
|
Porphyria, Acute Intermittent, Nonerythroid Variant |
Chain1295 |
This is a rare disease. |
|
Porphyria, Acute Intermittent |
Chain1294 |
This is a rare disease. |
|
Porphyria, Acute Hepatic |
Chain1293 |
This is a rare disease. |
|
Porphyria Cutanea Tarda |
Chain1292 |
This is a rare disease. |
|
Poor Paclitaxel Metabolism |
Chain1291 |
This is a rare disease. |
|
Polymorphism that May Influence odds ratio of Crohn's disease when in cis with Other CARD15 Mutations |
Chain1290 |
This is a rare disease. |
|
Polymicrogyria, Bilateral Frontoparietal |
Chain1289 |
This is a rare disease. |
|
Polycythemia, Chuvash Type |
Chain1288 |
This is a rare disease. |
|
Polycythemia Vera |
Chain1287 |
This is a rare disease. |
|
Polycystic kidney disease 1 |
Chain1285 |
This is a rare disease. |
|
Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy |
Chain1286 |
This is a rare disease. |
|
Polycystic Kidney Disease |
Chain1284 |
This is a rare disease. |
|
Platelet Glycoprotein IV Deficiency |
Chain1283 |
This is a rare disease. |
|
Placental Aromatase deficiency |
Chain1282 |
This is a rare disease. |
|
Pitt-Hopkins Syndrome |
Chain1281 |
This is a rare disease. |
|
Pigmented Paravenous Chorioretinal Atrophy |
Chain1280 |
This is a rare disease. |
