Human Disease and Mouse Model Detail
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Human Disease
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Microcephaly, Amish Type; MCPHA
OMIM ID: 607196
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Synonyms
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Amish Lethal Microcephaly;
Thiamine Metabolism Dysfunction Syndrome 3 (microcephaly Type); THMD3
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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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Slc25a19*
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SLC25A19*
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View 1 model
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1:1 Homology
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Mouse Models
Human Disease Modeled: Microcephaly, Amish Type; MCPHA
Associated Mouse Gene:
Slc25a19
Analysis Tools