Pages that link to "Autosomal recessive multiple epiphyseal dysplasia"
Showing 50 items.
- Achondroplasia (links | edit)
- Osteosclerosis (links | edit)
- Osteopetrosis (links | edit)
- Osteogenesis imperfecta (links | edit)
- Hereditary multiple exostoses (links | edit)
- Ellis–Van Creveld syndrome (links | edit)
- Diastrophic dysplasia (links | edit)
- Atelosteogenesis, type II (links | edit)
- Fibrous dysplasia of bone (links | edit)
- Thanatophoric dysplasia (links | edit)
- Achondrogenesis (links | edit)
- Enchondroma (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)
- Léri–Weill dyschondrosteosis (links | edit)
- Osteochondrodysplasia (links | edit)
- Short rib–polydactyly syndrome (links | edit)
- Majewski's polydactyly syndrome (links | edit)
- Osteochondromatosis (links | edit)
- Rhizomelic chondrodysplasia punctata (links | edit)
- Conradi–Hünermann syndrome (links | edit)
- Chondrodysplasia punctata (links | edit)
- Ollier disease (links | edit)
- Maffucci syndrome (links | edit)
- Multiple epiphyseal dysplasia (links | edit)
- Jansen's metaphyseal chondrodysplasia (links | edit)
- Metaphyseal dysplasia (links | edit)
- Raine syndrome (links | edit)
- Enchondromatosis (links | edit)
- Osteopoikilosis (links | edit)
- Camurati–Engelmann disease (links | edit)
- Antley–Bixler syndrome (links | edit)
- Boomerang dysplasia (links | edit)
- Fibrochondrogenesis (links | edit)
- Metaphyseal chondrodysplasia Schmid type (links | edit)
- Osteochondroprogenitor cell (links | edit)
- Recessive multiple epiphyseal dysplasia (redirect page) (links | edit)
- Genetic disorder (links | edit)
- Crohn's disease (links | edit)
- Congenital disorder of glycosylation (links | edit)
- Fructose malabsorption (links | edit)
- Hyperinsulinemic hypoglycemia (links | edit)
- Cystinuria (links | edit)
- Pendred syndrome (links | edit)
- Diastrophic dysplasia (links | edit)
- Atelosteogenesis, type II (links | edit)
- Fuchs' dystrophy (links | edit)
- Gitelman syndrome (links | edit)
- Hartnup disease (links | edit)
- Salla disease (links | edit)
- Lysinuric protein intolerance (links | edit)
- Hereditary elliptocytosis (links | edit)
- Achondrogenesis type 1B (links | edit)
- African iron overload (links | edit)
- Chromosome 5 (links | edit)
- Nonsyndromic deafness (links | edit)
- Autosomal recessive multiple epiphyseal dysplasia (links | edit)
- Acrodermatitis enteropathica (links | edit)
- Testicular microlithiasis (links | edit)
- Solute carrier family (links | edit)
- Multiple epiphyseal dysplasia (links | edit)
- Episodic ataxia (links | edit)
- Thyroid dyshormonogenesis (links | edit)
- Arterial tortuosity syndrome (links | edit)
- Renal glycosuria (links | edit)
- Allan–Herndon–Dudley syndrome (links | edit)
- GLUT1 deficiency (links | edit)
- Sulfate transporter (links | edit)
- Glucose-galactose malabsorption (links | edit)
- Mitochondrial pyruvate carrier 2 (links | edit)
- Monocarboxylate transporter 1 (links | edit)
- Fanconi–Bickel syndrome (links | edit)
- Inborn errors of carbohydrate metabolism (links | edit)
- Iminoglycinuria (links | edit)
- Ichthyosis prematurity syndrome (links | edit)
- Congenital disorder of glycosylation type IIc (links | edit)
- SLC17A3 (links | edit)
- Mitochondrial pyruvate carrier 1 (links | edit)
- SPATCCM (links | edit)
- Template:Solute carrier disorders (links | edit)
- Achondroplasia in children (links | edit)
- Opsismodysplasia (links | edit)
- Mesomelia (links | edit)
- Spondyloenchondrodysplasia (links | edit)