Kosmix
One sec... we're building your guide for
Peutz-jeghers Syndrome
Peutz-jeghers syndrome
Overview
Health Providers & Organizations
Main ›
Related in the Kosmos
?
Melanocytic nevi and neoplasms
Lentiginosis
FAMMM
Carney complex
Disturbances of human pigmentation
Melanism
Pigmentation disorders
Syndromes
(8)
HNPCC
Juvenile polyposis syndrome
Abdallat Davis Farrage syndrome
Hereditary sensory and autonomic neuropathies
Fetofetal transfusion
Fetofetal transfusion
Li-fraumeni syndrome
Gardner syndrome
Lentiginosis
more...
Gastroenterology
Polyposis
Intussusception (medical disorder)
Colorectal polyps
Cronkhite-Canada syndrome
Digestive system diseases
Gastric polyps
Oncology
(9)
Adenomatous
Tumor suppressor gene
Pancreatic ductal carcinoma
Neoplasia
Juvenile polyposis syndrome
Juvenile polyposis syndrome
Colorectal polyps
Cronkhite-Canada syndrome
FAMMM
Gardner syndrome
more...
Gynecology
Hereditary breast-ovarian cancer syndrome
Polyposis
Genetic disorders
(21)
Familial adenomatous polyposis
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Leukodystrophy, globoid cell
Ataxia telangiectasia
Ataxia telangiectasia
Bannayan-Zonana syndrome
Gaucher disease type 2
Galactosemias
Propionic acidemia
Pyruvate carboxylase deficiency
Otospondyl- omegaepiphyseal dysplasia
Long-chain 3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Basal cell nevus syndrome
Tuberous sclerosis
Pseudoxanthoma elasticum
Lentiginosis
Juvenile polyposis syndrome
Abdallat Davis Farrage syndrome
Hereditary sensory and autonomic neuropathies
Li-fraumeni syndrome
Gardner syndrome
more...
Hereditary cancers
(16)
Cowden syndrome
Attenuated familial adenomatous polyposis
Breast cancer
Carney complex
Familial adenomatous polyposis
Familial adenomatous polyposis
Gardner syndrome
HNPCC
Hereditary breast-ovarian cancer syndrome
Kidney cancer
Li-fraumeni syndrome
Multiple endocrine neoplasia
Multiple endocrine neoplasia type 2b
Retinoblastoma
Turcot syndrome
Von Hippel – Lindau disease
Xeroderma pigmentosum
more...
Gastrointestinal cancer
(37)
Anal cancer
Cancer of the pancreas
Cholangiocarcinoma
Duodenal cancer
Small bowel cancer
Small bowel cancer
Anal Pap smear
Appendix cancer
Attenuated familial adenomatous polyposis
Carcinoid
Colorectal cancer
Colorectal cancer survivors
Deaths from anal cancer
Deaths from colorectal cancer
Deaths from gallbladder cancer
Deaths from liver cancer
Deaths from pancreatic cancer
Deaths from small intestine cancer
Deaths from stomach cancer
Esophageal cancer
Familial adenomatous polyposis
Fibrolamellar hepatocellular carcinoma
Gallbladder cancer
Gardner syndrome
Gastric lymphoma
Gastrointestinal stromal tumor
HNPCC
Hepatocellular carcinoma
Intraductal papillary mucinous neoplasm
Klatskin tumor
Krukenberg tumor
Linitis plastica
MALT lymphoma
Pancreatic cancer survivors
Pancreatic ductal carcinoma
Pseudomyxoma peritonei
Squamous cell carcinoma
Stomach cancer
more...
Anatomical pathology
Hamartomatous
Hyperplastic
Adenomatous
Neoplasia
Tumor suppressor genes
(15)
Brca1
Brca2
APC (gene)
CDKN1B
Cyclin-dependent kinase inhibitor 1C
Cyclin-dependent kinase inhibitor 1C
PTEN (gene)
SDHB
SDHD
TCF21
TIG1
Tumor suppressor gene
Von Hippel-Lindau tumor suppressor
p16 (gene)
p53
p73
more...
Developmental biology
Congenital malformations
Germline
Processus vaginalis
Precocious puberty
Diseases and disorders
(53)
Paraquat lung
Polyglucosan body disease adult
Glossopharyngeal nerve diseases
Intestinal polyps
Type i complex regional pain syndrome
Type i complex regional pain syndrome
Myopathies, structural, congenital
Phakomatoses
Progressive osseous heteroplasia
Enterocolitis, pseudomembranous
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Intervertebral disk displacement
Rosenthal syndrome
Alzheimer disease type 2
Optic neuropathy, ischemic
Myotonic dystrophy type 2
Juvenile primary lateral sclerosis
Syndromes
Familial adenomatous polyposis
Hamartomatous
Lentiginosis
Juvenile polyposis syndrome
Cowden syndrome
Abdallat Davis Farrage syndrome
Hyperostosis, cortical, congenital
Purpura, schoenlein-henoch
Adenomatous
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Fetofetal transfusion
Ataxia telangiectasia
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Gaucher disease type 2
Galactosemias
Small bowel cancer
Brachial plexus neuropathies
Li-fraumeni syndrome
FAMMM
Melanism
Pyruvate carboxylase deficiency
Anal cancer
Basal cell nevus syndrome
Cancer of the pancreas
Gardner syndrome
Tuberous sclerosis
Lipomas
Precocious puberty
Muir-Torre syndrome
Pseudoxanthoma elasticum
more...
Signs and tests
(8)
Anemia
Clubbed fingers or toes
Complete blood count
Exostosis
Intussusception
Intussusception
Polyps biopsy
Stool guaiac test
X-ray of abdomen
more...
See also
(20)
Diseases and disorders
Secondary Parkinsons
STK11
Penis pain
Peutz
Peutz
Mucocutaneous
Macules
Purpura, schoenlein-henoch
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Chromosome 19
Serine-threonine kinase
Lipoprotein lipase deficiency, familial
Acor.org
Architects
Blood in stool
Cancer Genetics Services Directory
Chronic
Geneclinics.org
Genetic counseling
more...
more categories...
Health Providers & Organizations
›
Vitals.com
