Human Disease and Mouse Model Detail
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Human Disease
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Hypertrichosis Universalis Congenita, Ambras Type; HTC1
OMIM ID: 145701
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Synonyms
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Ambras Syndrome
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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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There are currently no human or mouse genes associated with this
disease in the MGI database.
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Transgenes and
other genome features
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Transgenes and other genome features developed in mice to model this disease.
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Mouse Models
Human Disease Modeled: Hypertrichosis Universalis Congenita, Ambras Type; HTC1
Associated Mouse Cytogenetic Marker:
In(15)4H
Analysis Tools