|
Osteogenesis Imperfecta, Type XIX (OI19) |
approved
|
301014 |
|
|
|
|
Osteopetrosis with Renal Tubular Acidosis (OPTB3) |
approved
|
259730 |
|
|
|
|
Osteopetrosis, Autosomal Recessive 5 (OPTB5) and Osteopetrosis, Infantile Malignant 3 |
approved
|
259720 |
|
|
Ostheopathia Striata with Cranial Sclerosis (OSCS) |
approved
|
300373 |
|
|
Otodental Dysplasia |
approved
|
166750 |
|
|
|
|
Otopalatodigital syndrome Type 2 (OPD2) |
approved
|
304120 |
|
|
Otopalatodigital type 1 |
approved
|
311300 |
|
|
|
|
Pachyonychia Congenita Type 1 |
approved
|
167200 |
|
|
|
|
Pachyonychia Congenita Type 2 |
approved
|
167210 |
|
|
|
|
Pachyonychia Congenita Type 3 |
approved
|
615726 |
|
|
|
|
Pachyonychia Congenita Type 4 |
approved
|
615728 |
|
|
|
|
Palmoplantar keratoderma, epidermolytic (EPPK) |
approved
|
144200 |
|
|
|
|
Palmoplantar keratoderma, non-epidermolytic (NEPPK) |
approved
|
600962 |
|
|
|
|
Palmoplantar Keratoderma, Nonepidermolytic, Focal or Diffuse |
approved
|
615735 |
|
|
|
|
Panhypopituitarism, X-linked; PHPX |
approved
|
312000 |
|
|
|
|
Paragangliomas 4 (PGL4) |
approved
|
115310 |
|
|
Paramyotonia Congenita (PMC) |
approved
|
168300 |
|
|
|
|
Paramyotonia Congenita of von Eulenburg |
approved
|
168300 |
|
|
Parathyroid Adenomatosis, Familial Cystic |
approved
|
145001 |
|
|
Parkinson’s disease 1 |
approved
|
168601 |
|
|
|
