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Ehlers-danlos Syndrome Type 1
Ehlers-danlos syndrome type 1
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Diseases and disorders
(39)
Ehlers Danlos Syndrome
Alport syndrome
Achondrogenesis type 2
Connective tissue disorder
Marfan syndrome
Marfan syndrome
Ehlers-danlos syndrome dermatosparaxis type
Schmid metaphyseal chondrodysplasia
Bullous pemphigoid
Osteogenesis imperfecta
Bethlem myopathy
Pelger-Huet anomaly
Ehlers-danlos syndrome type 3
Ehlers-danlos syndrome classic type
Epidermolysis bullosa dystrophica
Hypochondrogenesis
Marshall syndrome
Diaphragmatic hernia
Spondyloep- imetaphyseal dysplasia, Strudwick type
Lupus erythematosus, cutaneous
Charcot-Marie-Tooth disease, type 4
Enterocolitis, pseudomembranous
Cutis laxa
Pseudoxanthoma elasticum
Aneurysms
Stickler syndrome
Amyotrophic lateral sclerosis type 2
Umbilical hernia
Larsen syndrome
Dural ectasia
Apert syndrome
Myotonic dystrophy type 2
Muscle hypotonia
Peripheral artery disease
Orthostatic intolerance
Mitral valve prolapse
Autonomic dysfunction
Cerebral aneurysm
Atelosteogenesis type 2
Multiple epiphyseal dysplasia
more...
Contortion
Hypermobility
Contortionists
Ehlers Danlos Syndrome
Frontbend
Joint dislocation
Whiplash (medicine)
Abnormalities of dermal fibrous and elastic tissue
(19)
Acrodermatitis chronica atrophicans
Anetoderma
Blepharochalasis
Cutis laxa
Ehlers Danlos Syndrome
Ehlers Danlos Syndrome
Elastosis perforans serpiginosa
Gerodermia osteodysplastica
Homocystinuria
Linear focal elastosis
Marfan syndrome
Osteogenesis imperfecta
Perforating calcific elastosis
Pseudoxanthoma elasticum
Reactive perforating collagenosis
Stretch marks
Striae distensae
Ullrich disease
Verrucous perforating collagenoma
Wrinkly skin syndrome
more...
Diseases involving the fasciae
Ehlers Danlos Syndrome
Hypermobility
Marfan syndrome
Lupus erythematosus, cutaneous
Syndromes
(11)
Laminopathy
Buschke-Ollendorff syndrome
Barraquer-Simons Syndrome
Ehlers Danlos Syndrome
Hypermobility
Hypermobility
Alport syndrome
Marfan syndrome
Marshall syndrome
Stickler syndrome
Larsen syndrome
Apert syndrome
more...
Congenital disorders
Genetic disorders
Congenital bilateral absence of vas deferens
Ehlers Danlos Syndrome
Achondrogenesis type 2
Buschke-Ollendorff syndrome
Bethlem myopathy
Structural proteins
(26)
COL3A1
Elastic fibers
Keratins
Procollagen
Scleroprotein
Scleroprotein
Type I collagen
Type II collagen
Actin
Amyloid
Anchoring fibrils
Catenin
Claudin
Coilin
Collagen, type XVII, alpha 1
Elastin
Elaunin
Extensin
Fibrillin
Fibrillogenesis
Hydrolyzed collagen
Lamin
Osteolathyrism
ParM
Reticular fiber
Sclerotin
Spongin
more...
Rare diseases
(8)
Ichthyosis bullosa of siemens
Epidermolysis bullosa
Atelosteogenesis, type II
Barraquer-Simons Syndrome
Marshall syndrome
Marshall syndrome
Stickler syndrome
Larsen syndrome
Multiple epiphyseal dysplasia
more...
Hernias
(24)
Femoral hernia
Incisional hernia
Perineal hernia
Amyand's hernia
Bochdalek hernia
Bochdalek hernia
De Garengeot's hernia
Direct inguinal hernia
Epigastric hernia
Grynfeltt-Lesshaft hernia
Hernia
Hernia images
Herniorrhaphy
Hiatus hernia
Indirect inguinal hernia
Inguinal hernia
Internal hernia
Obturator hernia
Paraumbilical hernia
Petit's hernia
Richter's hernia
Shouldice Hernia Centre
Spigelian hernia
Stoppa operation
Umbilical hernia
more...
Gene
(9)
COL5A1
COL5A2
COL1A2
B4GALT7
COL11A1
COL11A1
Fibrillin 1
COL3A1
Type II collagen
Type I collagen
more...
Genetic disorders
(23)
Collagenopathy, types II and XI
Autosomal dominant polycystic kidney disease
Nonsyndromic deafness
Ehlers Danlos Syndrome
Alport syndrome
Alport syndrome
Laminopathy
Buschke-Ollendorff syndrome
Marfan syndrome
Barraquer-Simons Syndrome
Osteogenesis imperfecta
Bethlem myopathy
Ichthyosis bullosa of siemens
Pelger-Huet anomaly
Hypochondrogenesis
Marshall syndrome
Spondyloep- imetaphyseal dysplasia, Strudwick type
Charcot-Marie-Tooth disease, type 4
Pseudoxanthoma elasticum
Stickler syndrome
Larsen syndrome
Apert syndrome
Atelosteogenesis, type II
Multiple epiphyseal dysplasia
more...
See also
(20)
Keratinopathy
Dermatosparaxis
Kyphoscoliosis
Lysyl hydroxylase
Autosomal dominant
Autosomal dominant
Autosomal recessive
Ehlers-Danlos syndrome, vascular type
COL1A1
Tenascin X
ADAMTS2
Aortic dissection
Type VII
Aortic root
Fibrils
Type-V collagen
Inguinal hernias
Inguinal canal
X-linked recessive
Years
Sclerae
more...
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