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Barraquer-simons Syndrome
Barraquer-Simons Syndrome
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Related in the Kosmos
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Conditions of the subcutaneous fat
(29)
Adiposis dolorosa
Familial partial lipodystrophy
Lipodystrophy
Localized lipodystrophy
Acquired generalized lipodystrophy
Acquired generalized lipodystrophy
Acute erythema nodosum
Alpha-1 antitrypsin deficiency panniculitis
Centrifugal abdominal lipodystrophy
Chronic erythema nodosum
Cold panniculitis
Congenital generalized lipodystrophy
Cytophagic histiocytic panniculitis
Erythema nodosum
Factitial panniculitis
Gouty panniculitis
HIV-associated lipodystrophy
Lipoatrophia annularis
Lipodermat- osclerosis
Madelung's disease
Nodular vasculitis
Pancreatic panniculitis
Panniculitis
Post-steroid panniculitis
Sclerema neonatorum
Sclerosing lipogranuloma
Septal panniculitis
Subcutaneous fat necrosis of the newborn
Traumatic panniculitis
Weber–Christian disease
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Rare diseases
(8)
Malonic aciduria
Marshall syndrome
Raine syndrome
Fibrochondrogenesis
Atelosteogenesis, type II
Atelosteogenesis, type II
Multiple epiphyseal dysplasia
Epidermolytic hyperkeratosis
Stickler syndrome
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Syndromes
Laminopathy
Buschke-Ollendorff syndrome
Ehlers Danlos Syndrome
Alport syndrome
Marshall syndrome
Raine syndrome
Stickler syndrome
Genetic disorders
(22)
Mitochondrial trifunctional protein deficiency
Lecithin cholesterol acyltransferase deficiency
Bethlem myopathy
Pelger-Huet anomaly
Abetalipop- roteinemia
Abetalipop- roteinemia
Hypochondrogenesis
Hypoalphal- ipoproteinemia
Collagenopathy, types II and XI
Adrenoleuk- odystrophy
Tangier disease
Achondroplasia
Malonic aciduria
Laminopathy
Buschke-Ollendorff syndrome
Marshall syndrome
Ehlers Danlos Syndrome
Alport syndrome
Raine syndrome
Fibrochondrogenesis
Atelosteogenesis, type II
Multiple epiphyseal dysplasia
Stickler syndrome
more...
Tissues
Keratinopathy
Hypertrophy
Subcutaneous fat
Inborn errors of metabolism
Malonic aciduria
Mitochondrial trifunctional protein deficiency
Lecithin cholesterol acyltransferase deficiency
Tangier disease
Skin conditions resulting from errors in metabolism
Apolipoprotein B deficiency
Combined hyperlipidemia
Xanthoma
Lipoid proteinosis
Adrenoleuk- odystrophy
Tangier disease
Congenital disorders
(8)
Achondrogenesis type 2
Achondrogenesis type 1B
Achondrogenesis
Congenital malformations
Buschke-Ollendorff syndrome
Buschke-Ollendorff syndrome
Bethlem myopathy
Ehlers Danlos Syndrome
Fibrochondrogenesis
more...
Lipid disorders
(15)
Familial hyperchole- sterolemia
Hyperlipop- roteinemia
Blood lipids
Cholesterol
Cholesterol Depletion
Cholesterol Depletion
Combined hyperlipidemia
High-density lipoprotein
Hyperchole- sterolemia
Hyperglyceridemia
Hypocholesterolemia
Lipoprotein lipase deficiency
Lipoprotein(a)
Low-density lipoprotein
Mevalonate inhibition
Triglyceride
more...
Diseases and disorders
(10)
Schmid metaphyseal chondrodysplasia
Lipoatrophic diabetes
Osteochondropathy
Osteochond- rodysplasia
Syndromes
Syndromes
Lecithin cholesterol acyltransferase deficiency
Bethlem myopathy
Pelger-Huet anomaly
Epidermolysis bullosa dystrophica
Raine syndrome
more...
Medical condition
(29)
Ichthyosis bullosa of siemens
Steatocystoma multiplex
Chondromatous
Dermatitis herpetiformis
Malonic aciduria
Malonic aciduria
Mitochondrial trifunctional protein deficiency
Achondrogenesis type 2
Adiposis dolorosa
Bethlem myopathy
Pelger-Huet anomaly
Marshall syndrome
Abetalipop- roteinemia
Hypochondrogenesis
Ehlers Danlos Syndrome
Epidermolysis bullosa dystrophica
Alport syndrome
Raine syndrome
Hypolipoproteinemia
Fibrochondrogenesis
Multiple epiphyseal dysplasia
Mandibuloacral dysplasia
Tangier disease
Bullous pemphigoid
Lipodystrophy
Osteochond- rodysplasia
Xanthoma
Hyperlipop- roteinemia
Stickler syndrome
Achondroplasia
more...
See also
(20)
Scleroprotein
Lipoid proteinosis
Acyl CoA dehydrogenase
Enzymes
Epidermolysis bullosa dystrophica
Epidermolysis bullosa dystrophica
Hypobetali- poproteinemia
Hyperglyceridemia
Hypolipoproteinemia
Mandibuloacral dysplasia
COL2A1 gene
Long chain
Bullous pemphigoid
Autosomal dominant
Autosomal recessive
Autoimmune
Lipoprotein
Beta oxidation
Carnitine
Type II collagen
Metabolism
more...
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