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7q31 microdeletion syndrome
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Childhood apraxia of speech
Intellectual disability-severe speech delay-mild dysmorphism syndrome
MALT lymphoma
Precursor B-cell acute lymphoblastic leukemia
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome
Synonym(s):
- Del(7)(q31)
- Monosomy 7q31
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
FOXP2 O15409605317
No signs/symptoms info available.