Pages that link to "Camurati–Engelmann disease"
From WikiMD's Food, Medicine & Wellness Encyclopedia
The following pages link to Camurati–Engelmann disease:
Displayed 46 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- McCune–Albright syndrome (← links | edit)
- List of OMIM disorder codes (← links | edit)
- List of diseases (C) (← links | edit)
- Genetic disorder (← links | edit)
- Osteodystrophy (← links | edit)
- Osteopetrosis (← links | edit)
- Rhizomelic chondrodysplasia punctata (← links | edit)
- Thanatophoric dysplasia (← links | edit)
- Waardenburg syndrome (← links | edit)
- Maffucci syndrome (← links | edit)
- Swyer syndrome (← links | edit)
- Miscellaneous (← links | edit)
- Metaphyseal chondrodysplasia Schmid type (← links | edit)
- Antley–Bixler syndrome (← links | edit)
- Camurati–Engelmann disease (transclusion) (← links | edit)
- Léri–Weill dyschondrosteosis (← links | edit)
- Health-encyclopedia-C (← links | edit)
- Template:Osteochondrodysplasia (← links | edit)
- Boomerang dysplasia (← links | edit)
- CED (redirect page) (← links | edit)
- List of rare diseases-C (← links | edit)
- Genetic diseases-C (← links | edit)
- Diaphyseal dysplasia 1, progressive (redirect page) (← links | edit)
- Diaphyseal sclerosis, multiple (redirect page) (← links | edit)
- DPD1 (redirect page) (← links | edit)
- Engelmann disease (redirect page) (← links | edit)
- List of rare diseases-E (← links | edit)
- Genetic diseases-E (← links | edit)
- Hereditary multiple diaphyseal sclerosis (redirect page) (← links | edit)
- Multiple diaphyseal sclerosis (redirect page) (← links | edit)
- Spondyloepiphyseal dysplasia congenita (← links | edit)
- Ollier disease (← links | edit)
- Osteogenesis imperfecta (← links | edit)
- Fibrochondrogenesis (← links | edit)
- Craniofrontonasal dysplasia (← links | edit)
- Achondrogenesis (← links | edit)
- Leri Weill dyschondrosteosis (← links | edit)
- Template:Extracellular ligand disorders (← links | edit)
- Atelosteogenesis type 2 (← links | edit)
- Achondroplasia (← links | edit)
- X-linked dominant chondrodysplasia punctata 2 (← links | edit)
- Hereditary multiple osteochondromas (← links | edit)
- Osteogenesis imperfecta type III (← links | edit)
- Osteogenesis imperfecta type VI (← links | edit)
- Jansen type metaphyseal chondrodysplasia (← links | edit)
- OSMED Syndrome (← links | edit)
- Osteogenesis imperfecta type II (← links | edit)
- Osteogenesis imperfecta type V (← links | edit)
- Osteopetrosis autosomal dominant type 1 (← links | edit)
- Dictionary-of-medicine-C (← links | edit)