Multiple hamartoma syndrome

Multiple hamartoma syndrome
Cowden's disease is inherited as an autosomal dominant trait.

Cowden Syndrome: Also known as Multiple Hamartoma Syndrome. Affects primarily women, causes skin rashes, tiny wart-like bumps, thyroid disease, and severe benign fibrocystic disease.

Multiple Hamartoma syndrome see Cowden disease
Multiple Hereditary Exostoses see Hereditary Multiple Exostoses
Multiple Myeloma see Leukaemia and other Allied Blood disorders
Multiple Osteochondromatosis see Hereditary Multiple Exostoses ...

multiple hamartoma syndrome
multiple lentigines syndrome
multiple mucosal neuroma syndrome
munchausen syndrome
munchhausen syndrome
murine acquired immunodeficiency syndrome
myasthenic syndrome
myelodysplastic syndrome ...

See also: Hamartoma, Carcinoma, Dysplasia, Deficiency, Arthritis