Genetic Non-Syndromic Renal or Urinary Tract Malformation disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

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Aliases & Classifications for Genetic Non-Syndromic Renal or Urinary Tract Malformation

MalaCards integrated aliases for Genetic Non-Syndromic Renal or Urinary Tract Malformation:

Name: Genetic Non-Syndromic Renal or Urinary Tract Malformation ⁵⁸

Classifications:

MalaCards categories:
Global: Rare diseases
Anatomical: Nephrological diseases

See all MalaCards categories (disease lists)

External Ids:

Orphanet ⁵⁸ ORPHA357506

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Summaries for Genetic Non-Syndromic Renal or Urinary Tract Malformation

MalaCards based summary : Genetic Non-Syndromic Renal or Urinary Tract Malformation

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Related Diseases for Genetic Non-Syndromic Renal or Urinary Tract Malformation

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Symptoms & Phenotypes for Genetic Non-Syndromic Renal or Urinary Tract Malformation

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Drugs & Therapeutics for Genetic Non-Syndromic Renal or Urinary Tract Malformation

Search Clinical Trials , NIH Clinical Center for Genetic Non-Syndromic Renal or Urinary Tract Malformation

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Genetic Tests for Genetic Non-Syndromic Renal or Urinary Tract Malformation

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Anatomical Context for Genetic Non-Syndromic Renal or Urinary Tract Malformation

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Publications for Genetic Non-Syndromic Renal or Urinary Tract Malformation

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Genes for Genetic Non-Syndromic Renal or Urinary Tract Malformation

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Variations for Genetic Non-Syndromic Renal or Urinary Tract Malformation

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Expression for Genetic Non-Syndromic Renal or Urinary Tract Malformation

Search GEO for disease gene expression data for Genetic Non-Syndromic Renal or Urinary Tract Malformation.

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Pathways for Genetic Non-Syndromic Renal or Urinary Tract Malformation

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GO Terms for Genetic Non-Syndromic Renal or Urinary Tract Malformation

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Sources for Genetic Non-Syndromic Renal or Urinary Tract Malformation

¹ BioSystems

² BitterDB

³ CDC

⁴ Cell Signaling Technology

⁵ ClinicalTrials

⁶ ClinVar

⁷ CNVD

⁸ Cochrane Library

⁹ Cosmic

¹⁰ dbSNP

¹¹ DGIdb

¹² Disease Ontology

¹³ diseasecard

¹⁴ DiseaseEnhancer

¹⁵ DISEASES

¹⁶ DrugBank

¹⁷ EFO

¹⁸ ExPASy

¹⁹ FMA

²⁰ GeneAnalytics

²¹ GeneCards

²² GeneGo (Thomson Reuters)

²³ GeneHancer via GeneCards

²⁴ GeneReviews

²⁵ Genetics Home Reference

²⁶ GenomeRNAi

²⁷ GEO DataSets

²⁸ GO

²⁹ GTR

³⁰ HMDB

³¹ HPO

³² ICD10

³³ ICD10 via Orphanet

³⁴ ICD9CM

³⁵ IUPHAR

³⁶ KEGG

³⁷ LifeMap

³⁸ LncRNADisease

³⁹ LOVD

⁴⁰ MalaCards

⁴¹ MedGen

⁴² MedlinePlus

⁴³ MeSH

⁴⁴ MESH via Orphanet

⁴⁵ MGI

⁴⁶ miR2Disease

⁴⁷ NCBI Bookshelf

⁴⁸ NCI

⁴⁹ NCIt

⁵⁰ NDF-RT

⁵¹ NIH Clinical Center

⁵² NIH Rare Diseases

⁵³ NINDS

⁵⁴ Novoseek

⁵⁵ Novus Biologicals

⁵⁶ OMIM

⁵⁷ OMIM via Orphanet

⁵⁸ Orphanet

⁵⁹ PathCards

⁶⁰ PharmGKB

⁶¹ PubMed

⁶² PubMed Health

⁶³ QIAGEN

⁶⁴ R&D Systems

⁶⁵ Reactome

⁶⁶ Sino Biological

⁶⁷ SNOMED-CT

⁶⁸ SNOMED-CT via HPO

⁶⁹ TGDB

⁷⁰ Tocris

⁷¹ UMLS

⁷² UMLS via Orphanet

⁷³ UniProtKB/Swiss-Prot

⁷⁴ Wikipedia