Human Disease and Mouse Model Detail
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Human Disease
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Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive; ECTD10B
OMIM ID: 224900
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Synonyms
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Ectodermal Dysplasia, Anhidrotic; EDA;
Ectodermal Dysplasia, Hypohidrotic; HED
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View all models
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View ALL (2) 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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Edar*
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EDAR*
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View 2 models
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1:1 Homology
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Mouse Models
Human Disease Modeled: Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive; ECTD10B
Associated Mouse Gene:
Edar
Analysis Tools