MCID: SLC010
MIFTS: 6

Salcedo Syndrome

Categories: Rare diseases, Nephrological diseases

Aliases & Classifications for Salcedo Syndrome

MalaCards integrated aliases for Salcedo Syndrome:

Name: Salcedo Syndrome 53 73
Glomerular Basement Membrane Disease, Nail-Patella Syndrome Type 53
Nail Patella Like Renal Disease 53

Classifications:



External Ids:

UMLS 73 C0403548

Summaries for Salcedo Syndrome

NIH Rare Diseases : 53 The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.Orpha Number: 2613Disease definitionNail-patella-like renal disease is a severe nephropathy characterised by renal dysfunction, proteinuria, oedema and microscopic haematuria. It has been described in three brothers, two of which died from end-stage renal insufficiency.Visit the Orphanet disease page for more resources.

MalaCards based summary : Salcedo Syndrome, also known as glomerular basement membrane disease, nail-patella syndrome type, is related to nail-patella-like renal disease.

Related Diseases for Salcedo Syndrome

Diseases related to Salcedo Syndrome via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 nail-patella-like renal disease 11.1

Symptoms & Phenotypes for Salcedo Syndrome

Drugs & Therapeutics for Salcedo Syndrome

Search Clinical Trials , NIH Clinical Center for Salcedo Syndrome

Genetic Tests for Salcedo Syndrome

Anatomical Context for Salcedo Syndrome

Publications for Salcedo Syndrome

Variations for Salcedo Syndrome

Expression for Salcedo Syndrome

Search GEO for disease gene expression data for Salcedo Syndrome.

Pathways for Salcedo Syndrome

GO Terms for Salcedo Syndrome

Sources for Salcedo Syndrome

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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