Additional Disease Briefs


galactosialidosis

Also known as: GSL, Goldberg syndrome, PPCA deficiency, cathepsin A deficiency, cathepsin A deficiency of, galactosialidosis, lysosomal protective Protein deficiency, lysosomal protective protein deficiency of, neuraminidase deficiency with beta-galactosidase deficiency, neuraminidase/Beta-galactosidase expression, protective Protein/Cathepsin a deficiency


gallbladder cancer

Also known as: cancer of gall bladder, gall bladder cancer, gallbladder Ca, gallbladder neoplasm, localised malignant gallbladder neoplasm, localized malignant gallbladder neoplasm, malignant gall bladder neoplasm, malignant gallbladder neoplasm, malignant gallbladder tumor, malignant gallbladder tumour, malignant neoplasm of gall bladder, malignant neoplasm of gallbladder, malignant neoplasm of the gallbladder, malignant tumor of gallbladder, malignant tumor of the gallbladder, malignant tumour of gallbladder, malignant tumour of the gallbladder, tumor of the gallbladder, tumour of the gallbladder


gallbladder melanoma

Also known as: gall bladder melanoma, gall bladder melanoma (disease), gallbladder malignant melanoma, gallbladder melanoma, malignant melanoma of gallbladder, malignant melanoma of the gallbladder, melanoma (disease) of gall bladder, melanoma of gallbladder, melanoma of the gallbladder


gallbladder neuroendocrine tumor, grade 1/2

Also known as: gallbladder NET, gallbladder neuroendocrine tumor, gallbladder neuroendocrine tumour, gallbladder well differentiated endocrine tumor, gallbladder well differentiated endocrine tumor/carcinoma, gallbladder well differentiated endocrine tumour


gallbladder rhabdomyosarcoma

Also known as: gall bladder rhabdomyosarcoma, gall bladder rhabdomyosarcoma (disease), gallbladder rhabdomyosarcoma, rhabdomyosarcoma (disease) of gall bladder, rhabdomyosarcoma of gallbladder, rhabdomyosarcoma of the gallbladder


Galloway-Mowat syndrome 1

Also known as: GAMOS1, Galloway syndrome, Galloway-Mowat syndrome 1, cerebellar ataxia with intellectual disability, optic atrophy, and skin abnormalities, cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities, microcephaly, hiatal hernia, and nephrotic syndrome, nephrosis-microcephaly syndrome, nephrosis-neuronal dysmigration syndrome, spinocerebellar ataxia, autosomal recessive 5, spinocerebellar ataxia, autosomal recessive 5, formerly