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5p- Syndrome
5p- syndrome
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Syndromes
(12)
3-M Syndrome
Karyotype 47,XXX
4p- syndrome
Hereditary sensory and autonomic neuropathies
Fetofetal transfusion
Fetofetal transfusion
Karyotype 47,XYY
18p deletion syndrome
Distal Arthrogryposis, Type IIA
Craniofacial dysostosis
Cerebral gigantism
Syndrome
Charge syndrome
more...
Rare diseases
49 xxxxx syndrome
Leukodystrophy, globoid cell
5-oxoprolinuria
4-hydroxybutyric aciduria
Cerebrohepatorenal syndrome
Dyskeratosis congenita
Genetic disorders
(30)
MGA type II
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Partial monosomy
Galactosemias
Galactosemias
Trisomy
Spondyloep- imetaphyseal dysplasia, Strudwick type
Cerebrotendinous xanthomatosis
Kniest dysplasia
21 hydroxylase deficiency
Chromosomal deletion
Coffin-lowry syndrome
Cleidocranial dysplasia
Monosomy
Chromosome disorders
Genetic condition
Carnitine deficiency
Cystinosis
Karyotype 47,XXX
4p- syndrome
49 xxxxx syndrome
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Karyotype 47,XYY
18p deletion syndrome
5-oxoprolinuria
4-hydroxybutyric aciduria
Cerebrohepatorenal syndrome
Craniofacial dysostosis
Dyskeratosis congenita
more...
Diseases and disorders
(60)
Chromosome 5p- syndrome
Chromosome 5 trisomy 5p
Congenital hypomyelination
Glossopharyngeal nerve diseases
Purpura, schoenlein-henoch
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Camptomelic syndrome
Myopathies, structural, congenital
18p syndrome
Chromosome 9 trisomy
Chromosome 9 tetrasomy 9p
Enterocolitis, pseudomembranous
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
49xxxxy syndrome
Intervertebral disk displacement
Rosenthal syndrome
Brachial plexus neuropathies
Diencephalic syndrome
Chronic lobular hepatitis
Optic neuropathy, ischemic
Chronic Progressive External Ophthalmoplegia
5th disease
Trisomy 13/18
Cutis laxa
Mental retardation
Cytomegalovirus
Dwarfism
Chemical pneumonitis
Cystitis
3-M Syndrome
Karyotype 47,XXX
Syndromes
MGA type II
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Fetofetal transfusion
Karyotype 47,XYY
Partial monosomy
Distal Arthrogryposis, Type IIA
Galactosemias
Spondyloep- imetaphyseal dysplasia, Strudwick type
Cerebrotendinous xanthomatosis
Cerebrohepatorenal syndrome
Craniofacial dysostosis
Kniest dysplasia
Coffin-lowry syndrome
Cleidocranial dysplasia
Cerebral gigantism
Dyskeratosis congenita
Chromosome disorders
Charge syndrome
Carnitine deficiency
Cystinosis
more...
Genodermatoses
4p- syndrome
Distal Arthrogryposis, Type IIA
Craniofacial dysostosis
Dyskeratosis congenita
Leukodystrophies
Adrenoleuk- odystrophy
Alexander disease
Canavan disease
Cerebrohepatorenal syndrome
Leukodystrophy, globoid cell
Metachromatic leukodystrophy
Pelizaeus-- Merzbacher disease
Cytogenetics
(20)
Chromosome
Mixoploidy
Autosome
Chromosomal translocation
Chromosome disorders
Chromosome disorders
Colcemid
Fluorescent in situ hybridization
Fragile sites
Germ plasm
Homologous chromosome
Karyotype
Monosomy
Partial monosomy
Pseudoautosomal region
Robertsonian translocation
Synapsis
Tetrasomy
Trisomy
Uniparental disomy
X chromosome
more...
Chromosomes
Chromosome 5
Chromosome 18
Short arm
Chromosome
Chromosome disorders
Symptoms
Separated abdominal muscles
Single transverse palmar crease
Birth mass
Low-set ears
Microcephaly
Micrognathism
Mental retardation
See also
(20)
Genes on chromosome 5
Delta catenin
17-hydroxy- corticosteroids
Corticosteroids
17-OH-progesterone
17-OH-progesterone
UFC 24
Telomerase reverse transcriptase
Cryptogenic fibrosing alveolitis
Dentin dysplasia
17-ketosteroids
25-hydroxy vitamin D
Dysplasia
Cerebellar diseases
Campylobacter pylori
5-HT
Five pence (Irish decimal coin)
National Association of Working Women
Diastasis recti
Inguinal hernia
Www.fivepminus.org
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