Pages that link to "Rhizomelic chondrodysplasia punctata"
Showing 50 items.
- Genetic disorder (links | edit)
- Adrenoleukodystrophy (links | edit)
- Achondroplasia (links | edit)
- Osteosclerosis (links | edit)
- Osteopetrosis (links | edit)
- Osteogenesis imperfecta (links | edit)
- Hereditary multiple exostoses (links | edit)
- Zellweger syndrome (links | edit)
- Ellis–Van Creveld syndrome (links | edit)
- Diastrophic dysplasia (links | edit)
- Atelosteogenesis, type II (links | edit)
- Fibrous dysplasia of bone (links | edit)
- Mulibrey nanism (links | edit)
- Thanatophoric dysplasia (links | edit)
- Achondrogenesis (links | edit)
- Enchondroma (links | edit)
- Plasmalogen (links | edit)
- Osteodystrophy (links | edit)
- Osteochondroma (links | edit)
- Hypochondrogenesis (links | edit)
- Achondrogenesis type 2 (links | edit)
- Otospondylomegaepiphyseal dysplasia (links | edit)
- Spondyloepiphyseal dysplasia congenita (links | edit)
- Hypochondroplasia (links | edit)
- Achondrogenesis type 1B (links | edit)
- Polyostotic fibrous dysplasia (links | edit)
- Chondrodystrophy (links | edit)
- List of ICD-9 codes 740–759: congenital anomalies (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
- Autosomal recessive multiple epiphyseal dysplasia (links | edit)
- Refsum disease (links | edit)
- Léri–Weill dyschondrosteosis (links | edit)
- Peroxisomal disorder (links | edit)
- Osteochondrodysplasia (links | edit)
- Short rib–polydactyly syndrome (links | edit)
- Acatalasia (links | edit)
- Majewski's polydactyly syndrome (links | edit)
- Osteochondromatosis (links | edit)
- Rhizomelia (links | edit)
- Rhizomelic chondrodysplasia punctata (transclusion) (links | edit)
- Conradi–Hünermann syndrome (links | edit)
- Chondrodysplasia punctata (links | edit)
- Micrognathism (links | edit)
- Chondrodysplasia punctata, rhizomelic (redirect page) (links | edit)
- List of MeSH codes (C18) (links | edit)
- List of MeSH codes (C16) (links | edit)
- List of MeSH codes (C05) (links | edit)
- Glyceronephosphate O-acyltransferase (links | edit)
- Alkylglycerone phosphate synthase (links | edit)
- Ollier disease (links | edit)
- Maffucci syndrome (links | edit)
- Multiple epiphyseal dysplasia (links | edit)
- Mevalonate kinase deficiency (links | edit)