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Pelger-huet Anomaly
Pelger-Huet anomaly
Overview
Anatomy
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Genetic disorders
(16)
Laminopathy
Buschke-Ollendorff syndrome
Barraquer-Simons Syndrome
Bethlem myopathy
Marshall syndrome
Marshall syndrome
Hypochondrogenesis
Collagenopathy, types II and XI
Ehlers Danlos Syndrome
Alport syndrome
Raine syndrome
Fibrochondrogenesis
Atelosteogenesis, type II
Multiple epiphyseal dysplasia
Activated protein c resistance
Stickler syndrome
Achondroplasia
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Diseases and disorders
Schmid metaphyseal chondrodysplasia
Epidermolysis bullosa dystrophica
Osteochond- rodysplasia
Osteochondropathy
Bethlem myopathy
Raine syndrome
Activated protein c resistance
Medical condition
(21)
Achondrogenesis type 2
Ichthyosis bullosa of siemens
Greenberg dysplasia
May Hegglin Anomaly
Steatocystoma multiplex
Steatocystoma multiplex
Bullous pemphigoid
Chondromatous
Acute monocytic leukemia
Platelets
Bethlem myopathy
Marshall syndrome
Hypochondrogenesis
Ehlers Danlos Syndrome
Epidermolysis bullosa dystrophica
Alport syndrome
Raine syndrome
Fibrochondrogenesis
Multiple epiphyseal dysplasia
Osteochond- rodysplasia
Stickler syndrome
Achondroplasia
more...
Congenital disorders
(8)
Achondrogenesis type 1B
Achondrogenesis
Congenital
Achondrogenesis type 2
Buschke-Ollendorff syndrome
Buschke-Ollendorff syndrome
Bethlem myopathy
Ehlers Danlos Syndrome
Fibrochondrogenesis
more...
Syndromes
(8)
Laminopathy
Buschke-Ollendorff syndrome
Barraquer-Simons Syndrome
Marshall syndrome
Ehlers Danlos Syndrome
Ehlers Danlos Syndrome
Alport syndrome
Raine syndrome
Stickler syndrome
more...
Hematology
Toxic granulation
Neutrophilia
Laminopathy
Activated protein c resistance
Cell biology
Neutrophils
Cytosis
Nuclear envelope
Platelets
See also
(20)
Keratinopathy
Scleroprotein
Lamin B receptor
Granulocytes
COL2A1 gene
COL2A1 gene
ISO 3166-1
Epidermolytic hyperkeratosis
Autosomal dominant
Autosomal recessive
Autoimmune
Myeloid
Penia
Chromatin
Type II collagen
Phytohaemagglutinin
Inner membrane
Homozygous
Lymphocytes
Nucleic acid
Hereditary
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