Cone-rod dystrophy |
Chain386 |
This is a rare disease. |
Cone-rod Dystrophy 3 and Retinitis Pigmentosa 19 |
Chain387 |
This is a rare disease. |
Cone-rod Dystrophy 6 |
Chain388 |
This is a rare disease. |
Congenital Adrenal Hyperplasia due to Steroid-11 Beta-hydroxylase Deficiency |
Chain389 |
This is a rare disease. |
Congenital Afibrinogenemia Congenital Hypofibrinogenemia |
Chain390 |
This is a rare disease. |
Congenital Cataract |
Chain391 |
This is a rare disease. |
Congenital Disorder of Glycosylation, Type IIc |
Chain393 |
This is a rare disease. |
Congenital Disorder of Glycosylation, Type Ia |
Chain394 |
This is a rare disease. |
Congenital Disorder of Glycosylation, Type Ib |
Chain395 |
This is a rare disease. |
Congenital Disorder of Glycosylation, Type IIa |
Chain396 |
This is a rare disease. |
Congenital disorders of glycosylation type 1D |
Chain397 |
This is a rare disease. |
Congenital disorders of glycosylation type 1G |
Chain398 |
This is a rare disease. |
Congenital disorders of glycosylation type 1K |
Chain399 |
This is a rare disease. |
Congenital Erythropoietic Porphyria |
Chain401 |
This is a rare disease. |
Congenital Fast Channel Myasthenic Syndrome |
Chain402 |
This is a rare disease. |
Congenital Fast-channel Myasthenic Syndrome |
Chain403 |
This is a rare disease. |
Congenital heart defects |
Chain404 |
This is a rare disease. |
Congenital lipoid adrenal hyperplasia |
Chain408 |
This is a rare disease. |
Congenital Insensitivity to Pain Syndrome |
Chain407 |
This is a rare disease. |
Congenital Merosin Deficient Muscular Dystrophy |
Chain409 |
This is a rare disease. |
Congenital Muscular Dystrophy, Type 1C, with Neurologic Abnormalities |
Chain410 |
This is a rare disease. |
Congenital myasthenic syndrome |
Chain411 |
This is a rare disease. |
Congenital Myasthenic Syndrome associated with Acetylcholine Receptor Deficiency |
Chain412 |
This is a rare disease. |
Congenital Nephrosis 1, Finnish Type |
Chain413 |
This is a rare disease. |
Congenital Sick Sinus Syndrome |
Chain414 |
This is a rare disease. |
Congenital Slow Channel Myasthenic Syndrome |
Chain415 |
This is a rare disease. |
Congenital Stationary Nightblindness |
Chain416 |
This is a rare disease. |
Conjunctivitis, Ligneous |
Chain417 |
This is a rare disease. |
Connatal Pelizaeus-Merzbacher Disease |
Chain418 |
This is a rare disease. |
Contractural Arachnodactyly, Congenital |
Chain419 |
This is a rare disease. |
Cowden Disease Bannayan-Riley-Ruvalcaba Syndrome Macrocephaly/Autism Syndrome |
Chain426 |
This is a rare disease. |
Corticosteroid-binding Globulin Deficiency |
Chain423 |
This is a rare disease. |
Costello Syndrome |
Chain424 |
This is a rare disease. |
Cowden Disease Bannayan-Riley-Ruvalcaba Syndrome |
Chain425 |
This is a rare disease. |
Cpox Deficiency |
Chain427 |
This is a rare disease. |