Human Disease and Mouse Model Detail
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Human Disease
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Speech-Language Disorder 1; SPCH1
OMIM ID: 602081
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Synonyms
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Childhood Apraxia of Speech; CAS;
Developmental Verbal Dyspraxia; DVD;
Speech and Language Disorder with Orofacial Dyspraxia
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View all models
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View ALL (1) mouse models for this human disease.
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Foxp2*
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FOXP2*
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View 1 model
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1:1 Homology
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Mouse Models
Human Disease Modeled: Speech-Language Disorder 1; SPCH1
Associated Mouse Gene:
Foxp2
Analysis Tools