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 60
Monosomy 7q31 60
Del(7)(q31) 60

Characteristics:

Orphanet epidemiological data:

60
7q31 microdeletion syndrome
Inheritance: Not applicable; Prevalence: <1/1000000 (Worldwide); Age of onset: Infancy,Neonatal;

Classifications:



External Ids:

ICD10 via Orphanet 35 Q93.5
Orphanet 60 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
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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