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Intellectual disability-severe speech delay-mild dysmorphism syndrome
1 OMIM reference -
1 associated gene
7 connected diseases
No signs/symptoms info
Disease Type of connection
MALT lymphoma
Precursor B-cell acute lymphoblastic leukemia
7q31 microdeletion syndrome
Childhood apraxia of speech
Burkitt lymphoma
Precursor T-cell acute lymphoblastic leukemia
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
FOXP1 Q9H334605515
No signs/symptoms info available.