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Cronkhite-canada Syndrome
Cronkhite-Canada syndrome
Overview
Health Providers & Organizations
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Related in the Kosmos
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Gastroenterology
Polyposis
Peutz-jeghers syndrome
Gastric polyps
Colonic polyps
Malabsorption
Gastrointestinal
Polypectomy
Genodermatoses
Craniofacial dysostosis
Acrocephal- opolysyndactyly
Oncology
Turcot syndrome
Gardner syndrome
Dysplasia
Peutz-jeghers syndrome
Colonic polyps
Genetic disorders
(9)
Partial monosomy
Carnitine deficiency
Charcot-Marie Tooth Disease
Familial adenomatous polyposis
Craniofacial dysostosis
Craniofacial dysostosis
Acrocephal- opolysyndactyly
Turcot syndrome
Gardner syndrome
Peutz-jeghers syndrome
more...
Syndromes
Syndrome
Craniofacial dysostosis
Gardner syndrome
Peutz-jeghers syndrome
Pathology
Acanthocytosis
Astrocytoma
Colonic polyps
Anatomical pathology
Hamartomatous
Granulomatosis
Hyperplastic
Lesions
Chromosomes
(57)
Chromosome 10
Chromosome 11
Chromosome 18
Chromosome 3
Chromosome 4
Chromosome 4
Ring chromosome
AZF1
Allosome
Autosome
Centromere
Chromatid
Chromomere
Chromosomal inversion
Chromosomal translocation
Chromosome
Chromosome 1 (human)
Chromosome 12 (human)
Chromosome 13 (human)
Chromosome 14 (human)
Chromosome 15 (human)
Chromosome 16 (human)
Chromosome 17 (human)
Chromosome 19 (human)
Chromosome 2 (human)
Chromosome 20 (human)
Chromosome 21 (human)
Chromosome 22 (human)
Chromosome 5 (human)
Chromosome 6 (human)
Chromosome 7 (human)
Chromosome 8 (human)
Chromosome 9 (human)
Chromosome abnormality
Chromosome conformation capture
Chromosome engineering
Chromosome regions
Chromosome segregation
Derivative chromosome
Dicentric chromosome
Dyad (biology)
G banding
Human β-globin locus
Inchrosil
Isochromosome
Karyotype
Lampbrush chromosome
Locus (genetics)
Marker chromosome
Personalized medicine
Proline-Rich Coiled Coil 1
Satellite chromosome
Small supernumerary marker chromosome
Subtelomere
Syntelic
Telomere
X chromosome
Y chromosome
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Congenital disorders
Camptodactyly
Macrocephaly
Gastric polyps
Diseases and disorders
(27)
Congenital hypomyelination
Camptomelic syndrome
Chromosome 9 trisomy
Chromosome 9 tetrasomy 9p
Chromosome 5 trisomy 5p
Chromosome 5 trisomy 5p
Allergic granulomatous angiitis
Agenesis of corpus callosum
Acanthoche- ilonemiasis
Intestinal polyps
Cutis laxa
Anemia, hemolytic
Aniridia
Conjunctivitis
Craniosynostosis
Craniofacial dysostosis
Acrocephal- opolysyndactyly
Turcot syndrome
Hamartomatous
Gardner syndrome
Syndromes
Partial monosomy
Carnitine deficiency
Granulomatosis
Charcot-Marie Tooth Disease
Astrocytoma
Familial adenomatous polyposis
Macrocephaly
more...
See also
(16)
Diseases and disorders
alopecia cicatrisata
Ectodermal
Cowden syndrome
Hyperpigmentation
Hyperpigmentation
Anterior cruciate ligament
Atopic dermatitis
Acps
Pedunculated
Neil J. Gunther
Skin pigmentation
Case report
Autosomal dominant
Angioplasty
Cutaneous
Fingernail
more...
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