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Ichthyosis Bullosa of Siemens
Ichthyosis bullosa of Siemens
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Related in the Kosmos
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Genodermatoses
(8)
Epidermolytic hyperkeratosis
Epidermolysis bullosa dystrophica
Lelis syndrome
Epidermolysis bullosa simplex
Ichthyoses
Ichthyoses
Congenital ichthyosiform erythroderma
Junctional epidermolysis bullosa (medicine)
Ichthyosis vulgaris
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Rare diseases
(11)
Barraquer-Simons Syndrome
Marshall syndrome
Raine syndrome
Fibrochondrogenesis
Atelosteogenesis, type II
Atelosteogenesis, type II
Multiple epiphyseal dysplasia
Stickler syndrome
Epidermolytic hyperkeratosis
Lelis syndrome
Epidermolysis bullosa simplex
Congenital ichthyosiform erythroderma
more...
Genetic disorders
(18)
Laminopathy
Buschke-Ollendorff syndrome
Bethlem myopathy
Pelger-Huet anomaly
Collagenopathy, types II and XI
Collagenopathy, types II and XI
Ehlers Danlos Syndrome
Hypochondrogenesis
Alport syndrome
Achondroplasia
Barraquer-Simons Syndrome
Marshall syndrome
Lelis syndrome
Raine syndrome
Fibrochondrogenesis
Atelosteogenesis, type II
Multiple epiphyseal dysplasia
Congenital ichthyosiform erythroderma
Stickler syndrome
more...
Keratins
(31)
Cytokeratin
Keratin 1
Keratin 2A
Keratinopathy
Type II keratin
Type II keratin
Beta-keratin
Hair keratin
Keratin 10
Keratin 12
Keratin 13
Keratin 14
Keratin 15
Keratin 16
Keratin 17
Keratin 18
Keratin 19
Keratin 20
Keratin 21
Keratin 3
Keratin 4
Keratin 5
Keratin 6A
Keratin 6B
Keratin 6C
Keratin 7
Keratin 8
Keratin 9
Tonofibril
Type I hair keratin
Type I keratin
Type II hair keratin
more...
Structural proteins
Scleroprotein
Type II collagen
Keratins
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...
Cutaneous conditions
Erythroderma
Bullous pemphigoid
Skin disorder
Diseases and disorders
(26)
Schmid metaphyseal chondrodysplasia
Ichthyosis male hypogonadism
Steatocystoma multiplex
Osteochondropathy
Chondromatous
Chondromatous
Osteochond- rodysplasia
Achondrogenesis type 2
Bethlem myopathy
Pelger-Huet anomaly
Epidermolysis bullosa dystrophica
Ehlers Danlos Syndrome
Hypochondrogenesis
Marshall syndrome
Alport syndrome
Raine syndrome
Fibrochondrogenesis
Epidermolysis bullosa simplex
Ichthyoses
Multiple epiphyseal dysplasia
Erythroderma
Bullous pemphigoid
Ichthyosis vulgaris
Skin disorder
Stickler syndrome
Irritable bowel syndrome
Achondroplasia
more...
See also
(17)
Autosomal dominant
Autosomal recessive
Epidermis (skin)
COL2A1 gene
Hermann Werner Siemens
Hermann Werner Siemens
Meesmann juvenile epithelial corneal dystrophy
Autoimmune
Mutations
Transcription factor II E
Irritable bowel syndrome
Integument
Subcutaneous tissue
Blister
Codon
Gene cluster
Intermediate filaments
GlaxoSmithKline
more...
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