All diseases

OMIM ID
602081
OMIM term:
SPEECH-LANGUAGE DISORDER 1; SPCH1
Alternative terms:
CHILDHOOD APRAXIA OF SPEECH; CAS
DEVELOPMENTAL VERBAL DYSPRAXIA; DVD
SPEECH AND LANGUAGE DISORDER WITH OROFACIAL DYSPRAXIA
(∗) Location:
7q31.1  
(†) Associated OMIM genes:
FOXP2  
(‡) Associated MGI genes:
Foxp2  

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