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Buschke-ollendorff Syndrome
Buschke-Ollendorff syndrome
Overview
Anatomy
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Congenital disorders
Achondrogenesis type 2
Bethlem myopathy
Fibrochondrogenesis
Achondrogenesis type 1B
Achondrogenesis
Ehlers Danlos Syndrome
Congenital malformations
Syndromes
(8)
Laminopathy
Barraquer-Simons Syndrome
Marshall syndrome
Raine syndrome
Alport syndrome
Alport syndrome
Stickler syndrome
Syndrome
Ehlers Danlos Syndrome
more...
Genetic disorders
(16)
Pelger-Huet anomaly
Hypochondrogenesis
Collagenopathy, types II and XI
Atelosteogenesis, type II
Multiple epiphyseal dysplasia
Multiple epiphyseal dysplasia
Boomerang dysplasia
Achondroplasia
Laminopathy
Barraquer-Simons Syndrome
Bethlem myopathy
Marshall syndrome
Raine syndrome
Alport syndrome
Fibrochondrogenesis
Ehlers Danlos Syndrome
Stickler syndrome
more...
Structural proteins
(23)
Elastic fibers
Elastin
Scleroprotein
Type II collagen
Actin
Actin
Anchoring fibrils
Catenin
Coilin
Collagen
Collagen, type III, alpha 1
Collagen, type XVII, alpha 1
Extensin
Fibrillin
Fibrillogenesis
Hydrolyzed collagen
Keratins
Lamin
Osteolathyrism
ParM
Reticular fiber
Sclerotin
Spongin
Type-I collagen
more...
Rare diseases
(9)
Epidermolytic hyperkeratosis
Barraquer-Simons Syndrome
Marshall syndrome
Raine syndrome
Fibrochondrogenesis
Fibrochondrogenesis
Atelosteogenesis, type II
Multiple epiphyseal dysplasia
Boomerang dysplasia
Stickler syndrome
more...
Integumentary system
Cutaneous
Dermatology
Hair
Intrinsic and extrinsic aging
Nails
Human body
Keratinopathy
Connective tissue
Subcutaneous tissue
Diseases and disorders
(9)
Schmid metaphyseal chondrodysplasia
Osteopoikilosis
Epidermolysis bullosa dystrophica
Melorheostosis
Osteochondropathy
Osteochondropathy
Osteochond- rodysplasia
Bethlem myopathy
Pelger-Huet anomaly
Raine syndrome
more...
Medical condition
(22)
Ichthyosis bullosa of siemens
Steatocystoma multiplex
Antley-bixler syndrome
Bullous pemphigoid
Chondromatous
Chondromatous
Achondrogenesis type 2
Bethlem myopathy
Pelger-Huet anomaly
Hypochondrogenesis
Osteopoikilosis
Marshall syndrome
Epidermolysis bullosa dystrophica
Raine syndrome
Alport syndrome
Fibrochondrogenesis
Multiple epiphyseal dysplasia
Boomerang dysplasia
Melorheostosis
Osteochond- rodysplasia
Ehlers Danlos Syndrome
Stickler syndrome
Achondroplasia
more...
See also
COL2A1 gene
Autoimmune
Junctional epidermolysis bullosa (medicine)
Osseous
Autosomal dominant
Lesions
PMID
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