Noonan Syndrome Type 4 |
approved
|
610733 |
|
Noonan Syndrome Type 5 |
approved
|
611553 |
|
|
Noonan Syndrome Type 6 |
approved
|
613224 |
|
|
Noonan Syndrome Type 7 |
approved
|
613706 |
|
|
Noonan Syndrome Type 8 |
approved
|
615355 |
|
|
Noonan Syndrome Type 9 |
approved
|
616559 |
|
|
Norrie Disease |
approved
|
310600 |
|
|
Oculocutaneous Albinism Type 1A (OCA1A) |
approved
|
203100 |
|
Oculocutaneous Albinism Type 1B (OCA1B) |
approved
|
606952 |
|
Oculocutaneous albinism type 2 |
approved
|
203200 |
|
|
Oculodentodigital Dysplasia (ODDD) |
approved
|
164200 |
|
|
Oculodentodigital Dysplasia (ODDD) |
approved
|
257850 |
|
|
Olmsted Syndrome, X-Linked (OLMSX) |
approved
|
300918 |
|
|
Omenn Syndrome |
approved
|
603554 |
|
Optic Atrophy 1 (OPA1) |
approved
|
165500 |
|
|
Ornithine transcarbamylase deficiency (OTD) |
approved
|
311250 |
|
Orofaciodigital Syndrome 1 (OFD1) |
approved
|
311200 |
|
|
Orofaciodigital Syndrome 7 (OFD7) (Currently the gene for this condition is unknown and cannot be tested for. The condition is currently under review.) |
approved
|
608518 |
|
|
Orofaciodigital syndrome IV (OFD4) |
approved
|
258860 |
|
|
Orofaciodigital syndrome V (OFDS5) |
approved
|
174300 |
|
|