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Ichthyosis Bullosa of Siemens
Ichthyosis bullosa of Siemens
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Genodermatoses
Epidermolytic hyperkeratosis
Epidermolysis bullosa dystrophica
Lelis syndrome
Ichthyoses
Epidermolysis bullosa simplex
Ichthyosis vulgaris
Rare diseases
(10)
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
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Genetic disorders
(17)
Laminopathy
Buschke-Ollendorff syndrome
Bethlem myopathy
Pelger-Huet anomaly
Hypochondrogenesis
Hypochondrogenesis
Collagenopathy, types II and XI
Alport syndrome
Ehlers Danlos Syndrome
Achondroplasia
Barraquer-Simons Syndrome
Marshall syndrome
Raine syndrome
Fibrochondrogenesis
Atelosteogenesis, type II
Lelis syndrome
Multiple epiphyseal dysplasia
Stickler syndrome
more...
Keratins
(31)
Keratin 1
Keratin 2A
Keratinopathy
Type II keratin
Beta-keratin
Beta-keratin
Cytokeratin
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
Syndromes
(10)
Irritable bowel syndrome
Laminopathy
Buschke-Ollendorff syndrome
Barraquer-Simons Syndrome
Marshall syndrome
Marshall syndrome
Raine syndrome
Alport syndrome
Lelis syndrome
Ehlers Danlos Syndrome
Stickler syndrome
more...
Congenital disorders
(8)
Achondrogenesis type 2
Achondrogenesis type 1B
Achondrogenesis
Congenital malformations
Buschke-Ollendorff syndrome
Buschke-Ollendorff syndrome
Bethlem myopathy
Fibrochondrogenesis
Ehlers Danlos Syndrome
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
Hypochondrogenesis
Marshall syndrome
Epidermolysis bullosa dystrophica
Raine syndrome
Alport syndrome
Fibrochondrogenesis
Ichthyoses
Multiple epiphyseal dysplasia
Epidermolysis bullosa simplex
Erythroderma
Bullous pemphigoid
Ehlers Danlos Syndrome
Ichthyosis vulgaris
Skin disorder
Stickler syndrome
Irritable bowel syndrome
Achondroplasia
more...
See also
(20)
COL2A1 gene
Autosomal dominant
Autosomal recessive
Central American Integration System
J. Invest. Dermatol.
J. Invest. Dermatol.
Companies
Hermann Werner Siemens
Meesmann juvenile epithelial corneal dystrophy
Organizations
Autoimmune
Mutations
Montmorillonite
Epidermis (skin)
Transcription factor II E
ROOP
Integument
Dorothy Eady
Blister
Codon
PMID
more...
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