MCID: RTR015

Ret-Related Pheochromocytoma malady

Categories: Genetic diseases, Rare diseases, Endocrine diseases, Cancer diseases

Aliases & Classifications for Ret-Related Pheochromocytoma

About this section

Aliases & Descriptions for Ret-Related Pheochromocytoma:

Name: Ret-Related Pheochromocytoma 24

Classifications:



Summaries for Ret-Related Pheochromocytoma

About this section
MalaCards based summary: Ret-Related Pheochromocytoma An important gene associated with Ret-Related Pheochromocytoma is RET (Ret Proto-Oncogene).

Related Diseases for Ret-Related Pheochromocytoma

About this section

Symptoms for Ret-Related Pheochromocytoma

About this section

Drugs & Therapeutics for Ret-Related Pheochromocytoma

About this section

Interventional clinical trials:

Search ClinicalTrials, NIH Clinical Center for Ret-Related Pheochromocytoma

Genetic Tests for Ret-Related Pheochromocytoma

About this section

Genetic tests related to Ret-Related Pheochromocytoma:

id Genetic test Affiliating Genes
1 Ret-Related Pheochromocytoma24 RET

Anatomical Context for Ret-Related Pheochromocytoma

About this section

Animal Models for Ret-Related Pheochromocytoma or affiliated genes

About this section

Publications for Ret-Related Pheochromocytoma

About this section

Variations for Ret-Related Pheochromocytoma

About this section

Expression for genes affiliated with Ret-Related Pheochromocytoma

About this section
Search GEO for disease gene expression data for Ret-Related Pheochromocytoma.

Pathways for genes affiliated with Ret-Related Pheochromocytoma

About this section

GO Terms for genes affiliated with Ret-Related Pheochromocytoma

About this section

Sources for Ret-Related Pheochromocytoma

About this section
2CDC
6CNVD
10DGIdb
15ExPASy
16FDA
17FMA
26GTR
27HGMD
28HMDB
29ICD10
30ICD10 via Orphanet
31ICD9CM
32IUPHAR
33KEGG
36MedGen
38MeSH
39MESH via Orphanet
40MGI
43NCI
44NCIt
45NDF-RT
48NINDS
49Novoseek
51OMIM
52OMIM via Orphanet
56PubMed
57QIAGEN
62SNOMED-CT via Orphanet
66Tumor Gene Family of Databases
67UMLS
68UMLS via Orphanet