has material basis in germline mutation in FOXP2 childhood apraxia of speech https://www.malacards.org/card/isolated_childhood_apraxia_of_speech speech and language disorder with orofacial dyspraxia MEDGEN:152917 speech-language disorder 1 MONDO:0011184 SCTID:229703009 DOID:0111275 developmental verbal apraxia Orphanet:209908 childhood apraxia of speech speech-language disorder type 1 icd11.foundation:1590154825 SPCH1 developmental verbal dyspraxia ICD9:315.39 developmental apraxia of speech OMIM:602081 speech-language disorder-1 GARD:0012889 das UMLS:C0750927 articulatory apraxia CAS specific language disorder hereditary neurological disease