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Skeletal Disorders
Skeletal disorders
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Skeletal system
Osseous
Skeletal muscle
The skeletal system
Hypochondroplasia
Axial skeleton
Skeletal structures
Disability
Schizophrenia, disorganized
Congenital disorders
Muscular dystrophies
Congenital disorders
(9)
Achondrogenesis
Genetic disorders
Achondrogenesis type 1B
Fibrochondrogenesis
Achondrogenesis type 2
Achondrogenesis type 2
Amelia (birth defect)
Acheiropodia
Abdominal wall defect
Congenital malformations
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Autosomal recessive disorders
(12)
Antley-bixler syndrome
Otospondyl- omegaepiphyseal dysplasia
Mucopolysa- ccharidoses
Diastrophic dysplasia
Atelosteogenesis, type II
Atelosteogenesis, type II
Raine syndrome
Mucolipidoses
Nemaline myopathy
Hurler syndrome
Cerebro-oc- ulo-facio-skeletal syndrome
Fibrochondrogenesis
Acheiropodia
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Rare diseases
(12)
Multiple epiphyseal dysplasia
Boomerang dysplasia
Upington disease
Wallis Zieff Goldblatt syndrome
Stickler syndrome
Stickler syndrome
Osteochondritis dissecans
Antley-bixler syndrome
Fibrochondrogenesis
Atelosteogenesis, type II
Raine syndrome
Acheiropodia
Cerebro-oc- ulo-facio-skeletal syndrome
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Syndromes
(8)
Pfeiffer syndrome
Reactive arthritis
Antley-bixler syndrome
Raine syndrome
Wallis Zieff Goldblatt syndrome
Wallis Zieff Goldblatt syndrome
Hurler syndrome
Stickler syndrome
Cerebro-oc- ulo-facio-skeletal syndrome
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Growth disorders
Achondroplasia
Dwarfism
Hypochondroplasia
Osteology
(10)
Bone fracture
Bone healing
Forensic osteology
Harold Frost
Mechanostat
Mechanostat
Osseous
Osteosynthesis
Phosphate homeostasis
Skeletal system
The skeletal system
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Muscular disorders
(23)
Congenital myopathies
Mitochondrial myopathies
Myopathies
Arthrogryposis
Central core disease
Central core disease
Centronuclear myopathy
Chronic progressive external ophthalmoplegia
Diastasis recti
Inclusion body myositis
Laminopathy
Macrophagic myofasciitis
Metabolic myopathy
Muscular dystrophies
Myokmia
Nemaline myopathy
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Polymyositis
Thyrotoxic myopathy
Torticollis
Writer's cramp
X-linked myotubular myopathy
Zenker's degeneration
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Lysosomal storage diseases
(40)
Lysosomal storage disorders
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Krabbe disease
Lipid storage disorder
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidoses
Mucolipidosis type IV
Mucopolysa- ccharidoses
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
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Skeletal disorders
(8)
Aneurysmal bone cyst
Ollier disease
Coxa valga
Coxa vara
Osteomalacia
Osteomalacia
Avascular necrosis
Juvenile osteochondrosis
Osteochondritis dissecans
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Symptoms
Skeletal abnormalities
Skeletal deformities
Short arms and legs
Short stature
Diseases and disorders
(53)
Chondromatous
Osteochondropathy
Osteochond- rodysplasia
Skeletal dysplasias
Ainhum
Ainhum
Schmid metaphyseal chondrodysplasia
Maroteaux-Lamy syndrome
Arthropathies
Skin infection
Skeletal fluorosis
Cutis laxa
Bone disease
Infectious bone disease
Metabolic Bone Disease
Renal osteodystrophy
Serous meningitis
Syndromes
Hypochondrogenesis
Achondroplasia
Myopathies
Fibrochondrogenesis
Mucopolysa- ccharidoses
Diastrophic dysplasia
Raine syndrome
Achondrogenesis type 2
Congenital myopathies
Dwarfism
Ollier disease
Multiple epiphyseal dysplasia
Boomerang dysplasia
Amelia (birth defect)
Acheiropodia
Upington disease
Wallis Zieff Goldblatt syndrome
Coxa valga
Muscular dystrophies
Hypochondroplasia
Mucolipidoses
Chondrodysplasia punctata, rhizomelic
Coxa vara
Nemaline myopathy
Osteomalacia
Hurler syndrome
Brachydactyly
Arachnodactyly
Stickler syndrome
Avascular necrosis
Juvenile osteochondrosis
Mitochondrial myopathies
Cerebro-oc- ulo-facio-skeletal syndrome
Osteochondritis dissecans
Growth disorders
Reactive arthritis
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See also
(20)
Second cranial nerve
Scrofuloderma
Semivegetarian
Serous meningitis
Musculo-skeletal
Musculo-skeletal
Musculoskeletal system
Senile lentigines
Hypochondrogenesis
COL2A1 gene
Single palmar crease
Short stature
Respiratory system
Respiratory system disorders
Anticholinesterase
Type II collagen
Haemostatic drugs
Diphosponate
Chondrodysplasia punctata, rhizomelic
Am. J. Med. Genet.
Autosomal dominant
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