I think that more than the disease itself, it is the predisposition to a disease that can be transmitted by inheritance. This predisposition is generically caused by the presence of genetic mutations in important genes involved in a specific pathway, whose malfunction leads to the disease.
For example, the mutation of the gene BRCA1 confers predisposition to breast cancer and it is genetically transmitted. BRCA1 is a protein involved in the detection and repair of damaged DNA; therefore, if a cell with mutBRCA1 is exposed to "insults" that affect the DNA structure, it would not be able to repair the problem and it could become a "cancer" cell and later a "cancer" clone.
Antother example is given by the mutation of genes involved in maintaining the stability of our genome (MMR complex, checkpoint kinase), which could lead to hereditary colon cancer.
Finally, people with Li-Fraumeni syndrome have a mutated p53, which is a "tumour suppressor" protein, as it is able to get rid of lesions "pre-cancerous" cells. These people are predisposed to sarcomas, lymphomas, etc...
Hovever, it is not 100% certain that people with those mutations will develop the disease at some stage of their life, as most of these "mutations" are complicated by a great deal of interplay between genes and environment.
Hope it is not too complicated - I tried to use layman terms...
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