MCID: XCH002
MIFTS: 4

X Chromosome Number Anomaly

Categories: Fetal diseases, Rare diseases

Aliases & Classifications for X Chromosome Number Anomaly

MalaCards integrated aliases for X Chromosome Number Anomaly:

Name: X Chromosome Number Anomaly 58

Classifications:

Orphanet: 58  
Developmental anomalies during embryogenesis


External Ids:

Orphanet 58 ORPHA263714

Summaries for X Chromosome Number Anomaly

Related Diseases for X Chromosome Number Anomaly

Diseases in the Y Chromosome Number Anomaly family:

X Chromosome Number Anomaly

Diseases related to X Chromosome Number Anomaly via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 x chromosome number anomaly with male phenotype 12.5
2 x chromosome number anomaly with female phenotype 12.5

Symptoms & Phenotypes for X Chromosome Number Anomaly

Drugs & Therapeutics for X Chromosome Number Anomaly

Search Clinical Trials , NIH Clinical Center for X Chromosome Number Anomaly

Genetic Tests for X Chromosome Number Anomaly

Anatomical Context for X Chromosome Number Anomaly

Publications for X Chromosome Number Anomaly

Variations for X Chromosome Number Anomaly

Expression for X Chromosome Number Anomaly

Search GEO for disease gene expression data for X Chromosome Number Anomaly.

Pathways for X Chromosome Number Anomaly

GO Terms for X Chromosome Number Anomaly

Sources for X Chromosome Number Anomaly

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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