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Camurati-engelmann Disease
Camurati-Engelmann disease
Overview
Anatomy
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Skeletal disorders
Ollier disease
Engelmann syndrome
Hereditary multiple exostoses
Chondrodystrophy
Fibrous dysplasia
Craniosynostosis
Genetic disorders
(27)
Atelosteogenesis, type II
Fibrochondrogenesis
Raine syndrome
Boomerang dysplasia
Otospondyl- omegaepiphyseal dysplasia
Otospondyl- omegaepiphyseal dysplasia
Hypochondrogenesis
Spondyloepiphyseal dysplasia congenita
Buschke-Ollendorff syndrome
Laminopathy
Achondroplasia
Multiple epiphyseal dysplasia
5p- syndrome
Thanatophoric dysplasia
Craniofacial dysostosis
Hypochondroplasia
Carnitine deficiency
Charcot-Marie Tooth Disease
Partial trisomy
Pfeiffer syndrome
Osteopetrosis
Alport syndrome
Ehlers Danlos Syndrome
Genetic disorder
Engelmann syndrome
Hereditary multiple exostoses
Chondrodystrophy
Fibrous dysplasia
more...
Autosomal recessive disorders
Atelosteogenesis, type II
Fibrochondrogenesis
Raine syndrome
Otospondyl- omegaepiphyseal dysplasia
Chondrodystrophy
Carnitine deficiency
Rare diseases
(8)
Atelosteogenesis, type II
Fibrochondrogenesis
Raine syndrome
Boomerang dysplasia
Multiple epiphyseal dysplasia
Multiple epiphyseal dysplasia
5p- syndrome
Thanatophoric dysplasia
Osteopetrosis
more...
Congenital disorders
Achondrogenesis type 1B
Achondrogenesis type 2
Achondrogenesis
Camptodactyly
Fibrochondrogenesis
Buschke-Ollendorff syndrome
Ehlers Danlos Syndrome
Syndromes
(9)
Maffucci syndrome
Raine syndrome
Buschke-Ollendorff syndrome
Laminopathy
5p- syndrome
5p- syndrome
Craniofacial dysostosis
Pfeiffer syndrome
Alport syndrome
Ehlers Danlos Syndrome
more...
Skeletal system
Osseous
Diaphyses
Long bones
Skeletal disorders
Hypochondroplasia
Diseases and disorders
(10)
Schmid metaphyseal chondrodysplasia
Osteochondropathy
Osteochond- rodysplasia
Short rib-polydactyly syndrome
Osteopoikilosis
Osteopoikilosis
Metaphyseal dysplasia
Bone disease
Cutis laxa
Raine syndrome
Chondrodysplasia punctata, rhizomelic
more...
Medical condition
(34)
Chondromatous
Antley-bixler syndrome
Camptomelic syndrome
Enchondromatosis
Fibrochondrogenesis
Fibrochondrogenesis
Raine syndrome
Boomerang dysplasia
Achondrogenesis type 2
Chondrodysplasia punctata, rhizomelic
Osteochond- rodysplasia
Short rib-polydactyly syndrome
Hypochondrogenesis
Ollier disease
Osteopoikilosis
Spondyloepiphyseal dysplasia congenita
Achondroplasia
Maffucci syndrome
Multiple epiphyseal dysplasia
5p- syndrome
Hereditary multiple exostoses
Thanatophoric dysplasia
Craniofacial dysostosis
Hypochondroplasia
Chondrodystrophy
Dwarfism
Carnitine deficiency
Cutis laxa
Charcot-Marie Tooth Disease
Partial trisomy
Osteopetrosis
Fibrous dysplasia
Alport syndrome
Ehlers Danlos Syndrome
Craniosynostosis
more...
See also
(14)
Chondrodysplasia punctata, rhizomelic
Dysplasia
Keratinopathy
TGFB1
TGFBR1
TGFBR1
Theodor Wilhelm Engelmann
TGFBR2
Scleroprotein
Ring chromosome
Dwarfism
Transforming growth factor beta
Autosomal dominant
Classical electromagnetism
Thickening
more...
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