The following pages link to Multiple epiphyseal dysplasia
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Chondrodystrophy (links | edit)
- African iron overload (links | edit)
- Nonsyndromic deafness (links | edit)
- Chromosome 19 (links | edit)
- List of ICD-9 codes 740–759: congenital anomalies (links | edit)
- Platyspondylic lethal skeletal dysplasia, Torrance type (links | edit)
- Autosomal recessive multiple epiphyseal dysplasia (links | edit)
- Infantile cortical hyperostosis (links | edit)
- Acrodermatitis enteropathica (links | edit)
- Testicular microlithiasis (links | edit)
- Léri–Weill dyschondrosteosis (links | edit)
- Osteochondrodysplasia (links | edit)
- Short rib–polydactyly syndrome (links | edit)
- Solute carrier family (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)
- Sack–Barabas syndrome (links | edit)
- Ollier disease (links | edit)
- Maffucci syndrome (links | edit)
- Pseudoachondroplasia (links | edit)
- Episodic ataxia (links | edit)
- Jansen's metaphyseal chondrodysplasia (links | edit)
- Metaphyseal dysplasia (links | edit)
- Raine syndrome (links | edit)
- Dermatopathia pigmentosa reticularis (links | edit)
- Med (links | edit)
- Pachyonychia congenita (links | edit)
- Bethlem myopathy (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)
- Epidermolysis bullosa dystrophica (links | edit)
- Glucose-galactose malabsorption (links | edit)
- Enchondromatosis (links | edit)
- Cartilage oligomeric matrix protein (links | edit)
- Collagen disease (links | edit)
- Collagen, type IX, alpha 2 (links | edit)
- Collagen, type IX, alpha 3 (links | edit)
- Osteopoikilosis (links | edit)
- Fairbanks disease (redirect page) (links | edit)
- Mitochondrial pyruvate carrier 2 (links | edit)
- CRELD2 (links | edit)
- Monocarboxylate transporter 1 (links | edit)
- Camurati–Engelmann disease (links | edit)
- Antley–Bixler syndrome (links | edit)