Additional Disease Briefs

mast syndrome

Also known as: Mast syndrome, SPG21, autosomal recessive spastic paraplegia 21, autosomal recessive spastic paraplegia type 21, hereditary spastic paraplegia 21, mast syndrome, spastic paraplegia 21, autosomal recessive

mastocytoma

Also known as: mastocytoma

maternal 14q32.2 hypermethylation syndrome

maternal 14q32.2 microdeletion syndrome

Also known as: maternal del(14)(q32.2), maternal monosomy 14q32.2

maternal hyperthermia induced birth defects

Also known as: hyperthermia induced defects

maternal phenylketonuria

Also known as: hyperphenylalaninemic embryopathy, maternal PKU, maternal hyperphenylalaninemia, phenylketonuric embryopathy

maternal riboflavin deficiency

Also known as: RBFVD, maternal riboflavin deficiency, riboflavin deficiency

maternal uniparental disomy of chromosome 1

Also known as: UPD(1)mat, maternal uniparental disomy of chromosome type 1

maternal uniparental disomy of chromosome 13

Also known as: UPD(13)mat, maternal uniparental disomy of chromosome type 13