Bannayan-Riley-Ruvalcaba syndrome

Summary
Synonym
  • Bannayan-Zonana syndrome
  • Cowden syndrome 1
  • Riley-Smith syndrome
  • Ruvalcaba-Myhre-Smith syndrome
Definition
A Cowden syndrome that is characterized by macrocephaly, multiple noncancerous tumors and hamartomas, and dark freckles on the penis, and has_material_basis_in heterozygous germline mutation in the PTEN gene on chromosome 10q23.
Super Class
Cowden syndrome autosomal dominant disease
External Links
Disease Ontology
DOID:0050657
Mondo Disease Ontology
MeSH
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 1 - 10 of 26 in total
Gene ID Gene Symbol Description Source
38 ACAT1 acetyl-CoA acetyltransferase 1
176 ACAN aggrecan
414 ARSD arylsulfatase D
1298 COL9A2 collagen type IX alpha 2 chain
1583 CYP11A1 cytochrome P450 family 11 subfamily A member 1
1636 ACE angiotensin I converting enzyme
2876 GPX1 glutathione peroxidase 1
4153 MBL2 mannose binding lectin 2
4595 MUTYH mutY DNA glycosylase
4680 CEACAM6 CEA cell adhesion molecule 6
The Human Phenotype Ontology
Displaying entries 91 - 100 of 158 in total
HPO ID HPO Term
HP:0002007 Frontal bossing
HP:0002017 Nausea and vomiting
HP:0002126 Polymicrogyria
HP:0002167 Abnormality of speech or vocalization
HP:0002170 Intracranial hemorrhage
HP:0002194 Delayed gross motor development
HP:0002250 Abnormal large intestine morphology
HP:0002315 Headache
HP:0002652 Skeletal dysplasia
HP:0002665 Lymphoma
Displaying all 5 entries
Gene ID Gene Symbol Description
5290 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
5728 PTEN phosphatase and tensin homolog
6390 SDHB succinate dehydrogenase complex iron sulfur subunit B
6391 SDHC succinate dehydrogenase complex subunit C
6392 SDHD succinate dehydrogenase complex subunit D

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024