Kongenitale Dyshormonogene Hypothyreose mit Kropf (CDHG) Züchter the offspring will always inherit

the offspring will always inherit one Ay allele

Analysis of up to 220 genetic diseases

the presence of multiple variants on a single copy of the gene cannot be excluded

The dilution of black pigment results in blue or grey coat colour

muscular fibrosis with fat infiltrations and cardiomyopathy

Kongenitale Dyshormonogene Hypothyreose mit Kropf (CDHG) Züchter the offspring will always inheritCongenital dyshormonogenic hypothyroidism with goiter (CDHG) is an autosomal recessive disorder, caused by lymphocytic destruction or idiopathic atrophy of the thyroid gland. The clinical signs include growth delay, low intensity heart murmur, cough, exercise intolerance, goiter and dyshormonogenesis. Inheritance: autosomal recessive Mutation: SLC5A5 gene Genetic test: The method used for genetic testing is extremely accurate and allows complete