MCID: RNL057

Renal Tubular Dysgenesis, Agt-Related malady

Genetic diseases, Nephrological diseases, Rare diseases, Fetal diseases categories

Aliases & Classifications for Renal Tubular Dysgenesis, Agt-Related

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Aliases & Descriptions for Renal Tubular Dysgenesis, Agt-Related:

Name: Renal Tubular Dysgenesis, Agt-Related 20


Classifications:



Summaries for Renal Tubular Dysgenesis, Agt-Related

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MalaCards based summary: Renal Tubular Dysgenesis, Agt-Related An important gene associated with Renal Tubular Dysgenesis, Agt-Related is AGT (angiotensinogen (serpin peptidase inhibitor, clade A, member 8)).

Related Diseases for Renal Tubular Dysgenesis, Agt-Related

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Symptoms for Renal Tubular Dysgenesis, Agt-Related

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Drugs & Therapeutics for Renal Tubular Dysgenesis, Agt-Related

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Drug clinical trials:

Search ClinicalTrials for Renal Tubular Dysgenesis, Agt-Related

Search NIH Clinical Center for Renal Tubular Dysgenesis, Agt-Related

Genetic Tests for Renal Tubular Dysgenesis, Agt-Related

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Genetic tests related to Renal Tubular Dysgenesis, Agt-Related:

id Genetic test Affiliating Genes
1 Renal Tubular Dysgenesis, Agt-Related20 AGT

Anatomical Context for Renal Tubular Dysgenesis, Agt-Related

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Animal Models for Renal Tubular Dysgenesis, Agt-Related or affiliated genes

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Publications for Renal Tubular Dysgenesis, Agt-Related

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Variations for Renal Tubular Dysgenesis, Agt-Related

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Expression for genes affiliated with Renal Tubular Dysgenesis, Agt-Related

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Search GEO for disease gene expression data for Renal Tubular Dysgenesis, Agt-Related.

Pathways for genes affiliated with Renal Tubular Dysgenesis, Agt-Related

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Compounds for genes affiliated with Renal Tubular Dysgenesis, Agt-Related

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GO Terms for genes affiliated with Renal Tubular Dysgenesis, Agt-Related

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Sources for Renal Tubular Dysgenesis, Agt-Related

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2CDC
12ExPASy
13FDA
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
28IUPHAR
29KEGG
33MeSH
34MESH via Orphanet
35MGI
38NCI
39NCIt
40NDF-RT
43NINDS
44Novoseek
46OMIM
47OMIM via Orphanet
51PubMed
52QIAGEN
57SNOMED-CT via Orphanet
61UMLS
62UMLS via Orphanet