|
Cone Rod Dystrophy 21 (CORD 21) |
approved
|
616502 |
|
|
|
|
Cone Rod Dystrophy 3 (CORD3) |
approved
|
604232 |
|
|
|
|
Cone Rod Dystrophy 5 (CORD5) |
approved
|
600977 |
|
|
|
|
Cone Rod Dystrophy 6 (CORD6) |
approved
|
601777 |
|
|
|
|
Cone Rod Dystrophy 7 (CORD7) |
approved
|
603349 |
|
|
|
|
Cone Rod Dystrophy 9 (CORD9) |
approved
|
612775 |
|
|
|
|
Congenital Adrenal Hyperplasia (21 hydroxylase deficiency) |
approved
|
201910 |
|
|
Congenital Cataracts |
approved
|
601885 |
|
|
|
|
Congenital Contractual Arachnodactyly (Beals Syndrome) |
approved
|
121050 |
|
|
|
|
Congenital Deafness with inner ear agenesis, microtia and microdontia |
approved
|
610706 |
|
|
|
|
Congenital Disorder of Glycosylation type 1a (CDG1A) |
approved
|
212065 |
|
|
Congenital Disorder of Glycosylation type 1D (CDG1D) |
approved
|
601110 |
|
|
|
|
Congenital Dyserythropoietic Anaemia types 1a, 1b and 2 |
approved
|
224120, 615631, 224100 |
|
|
|
|
Congenital Fibrosis of the extraocular muscles (CFEOM1 and CFEOM3B) |
approved
|
135700 |
|
|
Congenital Heart Defects, Multiple Types 6 (CHTD6) (NB this relates to the autosomal recessive type of the condition only) |
approved
|
613854 |
|
|
|
|
Congenital hereditary cataract, type 10 (CTRCT10) |
approved
|
600881 |
|
|
|
|
Congenital hereditary cataract, type 11 (CTRCT11) |
approved
|
610623 |
|
|
|
|
Congenital hereditary cataract, type 12 (CTRCT12) |
approved
|
611597 |
|
|
|
|
Congenital hereditary cataract, type 15 (CTRCT15) |
approved
|
615274 |
|
|
|
|
Congenital hereditary cataract, type 16 (CTRCT16) |
approved
|
613763 |
|
|
|
