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childhood apraxia of speech

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Uniprot Description A disorder characterized by severe orofacial dyspraxia resulting in largely incomprehensible speech. Affected individuals have severe impairment in the selection and sequencing of fine orofacial movements which are necessary for articulation, and deficits in several facets of grammatical skills and language processing, such as the ability to break up words into their constituent phonemes.
Mondo Term and Equivalent IDs
MONDO:0011184:  childhood apraxia of speech
GARD:0012889: 
Orphanet:209908: 
SCTID:229703009: