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 59
Monosomy 7q31 59
Del(7)(q31) 59

Characteristics:

Orphanet epidemiological data:

59
7q31 microdeletion syndrome
Inheritance: Not applicable; Prevalence: <1/1000000 (Worldwide); Age of onset: Infancy,Neonatal;

Classifications:



External Ids:

Orphanet 59 ORPHA251061
ICD10 via Orphanet 34 Q93.5

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 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 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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