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Hypotrichosis is characterised by congenital hypotrichosis and short life expectancy.
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Specifications
| Breeds | |
|---|---|
| Gene | |
| Organ | |
| specimen | Swab, Blood EDTA, Blood Heparin, Semen, Tissue |
| Mode of Inheritance | |
| Chromosome | |
| Year Published |
General information
Hypotrichosis is characterised by congenital hypotrichosis and short life expectancy. The mode of inheritance is autosomal recessive. The disease has been described in the Birman cat breed. Hypotrichosis is mostly likely caused by a deletion in the FOXN1 gene.
Clinical features
Hypotrichosis with short life expectancy.
Additional information
References
Pubmed ID: 25781316
Omia ID: 1949
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