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 11 - 20 of 26 in total
Gene ID Gene Symbol Description Source
5290 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
5291 PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta
5293 PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta
5294 PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma
5728 PTEN phosphatase and tensin homolog
6319 SCD stearoyl-CoA desaturase
6382 SDC1 syndecan 1
6390 SDHB succinate dehydrogenase complex iron sulfur subunit B
6391 SDHC succinate dehydrogenase complex subunit C
6392 SDHD succinate dehydrogenase complex subunit D
The Human Phenotype Ontology
Displaying entries 71 - 80 of 158 in total
HPO ID HPO Term
HP:0000587 Abnormal optic nerve morphology
HP:0000615 Abnormal pupil morphology
HP:0000828 Abnormality of the parathyroid gland
HP:0000872 Hashimoto thyroiditis
HP:0000965 Cutis marmorata
HP:0001004 Lymphedema
HP:0001009 Telangiectasia
HP:0001028 Hemangioma
HP:0001031 Subcutaneous lipoma
HP:0001100 Heterochromia iridis
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