MCID: 7Q3001
MIFTS: 6

7q31 Microdeletion Syndrome

Categories: Fetal diseases, Rare diseases

Aliases & Classifications for 7q31 Microdeletion Syndrome

MalaCards integrated aliases for 7q31 Microdeletion Syndrome:

Name: 7q31 Microdeletion Syndrome 58
Monosomy 7q31 58
Del(7)(q31) 58

Characteristics:

Orphanet epidemiological data:

58
7q31 microdeletion syndrome
Inheritance: Not applicable; Prevalence: <1/1000000 (Worldwide); Age of onset: Infancy,Neonatal;

Classifications:

Orphanet: 58  
Developmental anomalies during embryogenesis


External Ids:

ICD10 via Orphanet 33 Q93.5
Orphanet 58 ORPHA251061

Summaries for 7q31 Microdeletion Syndrome

MalaCards based summary : 7q31 Microdeletion Syndrome, is also known as monosomy 7q31. An important gene associated with 7q31 Microdeletion Syndrome is FOXP2 (Forkhead Box P2).

Related Diseases for 7q31 Microdeletion Syndrome

Symptoms & Phenotypes for 7q31 Microdeletion Syndrome

Drugs & Therapeutics for 7q31 Microdeletion Syndrome

Search Clinical Trials , NIH Clinical Center for 7q31 Microdeletion Syndrome

Genetic Tests for 7q31 Microdeletion Syndrome

Anatomical Context for 7q31 Microdeletion Syndrome

Publications for 7q31 Microdeletion Syndrome

Variations for 7q31 Microdeletion Syndrome

Expression for 7q31 Microdeletion Syndrome

Search GEO for disease gene expression data for 7q31 Microdeletion Syndrome.

Pathways for 7q31 Microdeletion Syndrome

GO Terms for 7q31 Microdeletion Syndrome

Sources for 7q31 Microdeletion Syndrome

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
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
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Apr-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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