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Multiple Epiphyseal Dysplasia
Multiple epiphyseal dysplasia
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Rare diseases
(14)
Atelosteogenesis, type II
Fibrochondrogenesis
Raine syndrome
Boomerang dysplasia
Antley-bixler syndrome
Antley-bixler syndrome
Ichthyosis bullosa of siemens
Barraquer-Simons Syndrome
Marshall syndrome
Multiple sulfatase deficiency
Thanatophoric dysplasia
Hereditary multiple exostoses
Perthes disease
Stickler syndrome
Menkes syndrome
more...
Genetic disorders
(39)
Recessive multiple epiphyseal dysplasia
Achondroplasia
Otospondyl- omegaepiphyseal dysplasia
Hypochondrogenesis
Laminopathy
Laminopathy
Buschke-Ollendorff syndrome
Spondyloepiphyseal dysplasia congenita
Collagenopathy, types II and XI
Pseudoacho- ndroplasia
Fukuyama type muscular dystrophy
Ehlers Danlos Syndrome
Diastrophic dysplasia
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Pelger-Huet anomaly
Bethlem myopathy
Spondyloep- imetaphyseal dysplasia
Spondyloperipheral dysplasia
Osteogenesis imperfecta
Alport syndrome
Kniest dysplasia
Mitochondrial trifunctional protein deficiency
Hypochondroplasia
Muenke syndrome
Chondrodystrophy
Marfan syndrome
Ellis-van creveld syndrome
Cartilage hair hypoplasia
Atelosteogenesis, type II
Fibrochondrogenesis
Raine syndrome
Boomerang dysplasia
Antley-bixler syndrome
Ichthyosis bullosa of siemens
Barraquer-Simons Syndrome
Marshall syndrome
Multiple sulfatase deficiency
Thanatophoric dysplasia
Hereditary multiple exostoses
Stickler syndrome
more...
Diseases and disorders
(66)
Epiphyseal dysplasia multiple 4
Achondrogenesis type 2
Schmid metaphyseal chondrodysplasia
Chondrodysplasia punctata, rhizomelic
Osteochondropathy
Osteochondropathy
Chondromatous
Syndromes
Osteochond- rodysplasia
Short rib-polydactyly syndrome
Metaphyseal dysplasia
Osteopoikilosis
Ollier disease
Camurati engelmann disease
Metatropic dwarfism
Chondrodysplasia punctata
Atelosteogenesis type 2
Morvan disease
Epidermolysis bullosa dystrophica
Melnick-needles syndrome
Ehlers-danlos syndrome dermatosparaxis type
Multicentric reticulohi- stiocytosis
Osteochondromatosis
Pachydermo- periostosis
Enchondromatosis
Skeletal dysplasias
Maffucci syndrome
Arthropathy
Marinesco sjogren syndrome
Coxa vara
Myotonic dystrophy type 2
Myelodysplastic syndromes
Myotubular myopathy
Dysostosis
Neuropathic arthropathy
Steatocystoma multiplex
Hypoplasia
Fibrochondrogenesis
Raine syndrome
Boomerang dysplasia
Achondroplasia
Hypochondrogenesis
Spondyloepiphyseal dysplasia congenita
Pseudoacho- ndroplasia
Fukuyama type muscular dystrophy
Ehlers Danlos Syndrome
Diastrophic dysplasia
Marshall syndrome
Pelger-Huet anomaly
Bethlem myopathy
Spondyloep- imetaphyseal dysplasia
Multiple sulfatase deficiency
Thanatophoric dysplasia
Hereditary multiple exostoses
Osteogenesis imperfecta
Alport syndrome
Kniest dysplasia
Mitochondrial trifunctional protein deficiency
Perthes disease
Hypochondroplasia
Muenke syndrome
Chondrodystrophy
Stickler syndrome
Marfan syndrome
Menkes syndrome
Ellis-van creveld syndrome
Cartilage hair hypoplasia
more...
Autosomal recessive disorders
(13)
Recessive multiple epiphyseal dysplasia
Atelosteogenesis, type II
Fibrochondrogenesis
Raine syndrome
Otospondyl- omegaepiphyseal dysplasia
Otospondyl- omegaepiphyseal dysplasia
Antley-bixler syndrome
Diastrophic dysplasia
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Multiple sulfatase deficiency
Mitochondrial trifunctional protein deficiency
Chondrodystrophy
Ellis-van creveld syndrome
Cartilage hair hypoplasia
more...
Genetic disorder
Recessive multiple epiphyseal dysplasia
Buschke-Ollendorff syndrome
Fukuyama type muscular dystrophy
Spondyloperipheral dysplasia
Mitochondrial trifunctional protein deficiency
Congenital disorders
(9)
Achondrogenesis type 1B
Achondrogenesis
Achondrogenesis type 2
Fibrochondrogenesis
Buschke-Ollendorff syndrome
Buschke-Ollendorff syndrome
Ehlers Danlos Syndrome
Bethlem myopathy
Marinesco sjogren syndrome
Muenke syndrome
more...
Skeletal system
Ossification
Long bones
Skeletal disorders
Hypochondroplasia
Gene
COL9A2
COL9A3
COL9A1
Cartilage oligomeric matrix protein
Type II collagen
Musculoskeletal system
Epiphyseal
Pellegrini-Stieda syndrome
Femoral head
Ossification
Coxa vara
See also
(13)
Keratinopathy
Dysplasia
Scleroprotein
SLC26A2
COL2A1 gene
COL2A1 gene
Autosomal dominant
Autosomal recessive
Short stature
Mullerian duct
Dyschondroplasia
Bone diseases
X linked
Trevor disease
more...
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