MCID: SLG001
MIFTS: 6

Selig Benacerraf Greene Syndrome

Categories: Nephrological diseases, Rare diseases

Aliases & Classifications for Selig Benacerraf Greene Syndrome

MalaCards integrated aliases for Selig Benacerraf Greene Syndrome:

Name: Selig Benacerraf Greene Syndrome 52 71
Renal Dysplasia, Megalocystis, and Sirenomelia 52

Classifications:



External Ids:

UMLS 71 C2931041

Summaries for Selig Benacerraf Greene Syndrome

MalaCards based summary : Selig Benacerraf Greene Syndrome, also known as renal dysplasia, megalocystis, and sirenomelia, is related to renal hypodysplasia/aplasia 1 and sirenomelia.

Related Diseases for Selig Benacerraf Greene Syndrome

Diseases related to Selig Benacerraf Greene Syndrome via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 renal hypodysplasia/aplasia 1 10.4
2 sirenomelia 10.4
3 renal dysplasia 10.4

Symptoms & Phenotypes for Selig Benacerraf Greene Syndrome

Drugs & Therapeutics for Selig Benacerraf Greene Syndrome

Search Clinical Trials , NIH Clinical Center for Selig Benacerraf Greene Syndrome

Genetic Tests for Selig Benacerraf Greene Syndrome

Anatomical Context for Selig Benacerraf Greene Syndrome

Publications for Selig Benacerraf Greene Syndrome

Articles related to Selig Benacerraf Greene Syndrome:

# Title Authors PMID Year
1
Renal dysplasia, megalocystis, and sirenomelia in four siblings. 61
8475459 1993

Variations for Selig Benacerraf Greene Syndrome

Expression for Selig Benacerraf Greene Syndrome

Search GEO for disease gene expression data for Selig Benacerraf Greene Syndrome.

Pathways for Selig Benacerraf Greene Syndrome

GO Terms for Selig Benacerraf Greene Syndrome

Sources for Selig Benacerraf Greene Syndrome

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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