|
Combined Oxidative Phosphorylation Deficiency 1 |
Chain378 |
This is a rare disease. |
|
Combined Saposin Deficiency |
Chain379 |
This is a rare disease. |
|
Complement C2 Deficiency, Type II |
Chain380 |
This is a rare disease. |
|
Complement C3 Deficiency |
Chain381 |
This is a rare disease. |
|
Complement C5 Deficiency |
Chain382 |
This is a rare disease. |
|
Complete Adenine Phosphoribosyltransferase Deficiency, Icelandic Type |
Chain383 |
This is a rare disease. |
|
Complex 1 Deficiency |
Chain384 |
This is a rare disease. |
|
Complex III deficiency |
Chain385 |
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. |
|
Cone-rod dystrophy |
Chain386 |
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 IIa |
Chain396 |
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 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 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 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. |
|
Congenital bilateral absence of vas deferens |
Chain65 |
|
|
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 heart defects |
Chain404 |
This is a rare disease. |
|
Congenital lipoid adrenal hyperplasia |
Chain408 |
This is a rare disease. |
