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 53 72
Renal Dysplasia, Megalocystis, and Sirenomelia 53

Classifications:



External Ids:

UMLS 72 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. 38
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 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 TGDB
71 Tocris
72 UMLS
73 UMLS via Orphanet
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