Additional Disease Briefs
Also known as:
breast cystosarcoma phyllodes, breast phyllodes neoplasm, breast phyllodes tumor, cystosarcoma phyllodes of breast, cystosarcoma phyllodes of the breast, cystosarcoma phylloides - breast, cystosarcoma phylloides of the breast, phyllodes breast neoplasm, phyllodes breast tumor, phyllodes breast tumour, phyllodes neoplasm of breast, phyllodes neoplasm of the breast, phyllodes tumor of breast, phyllodes tumor of the breast, phyllodes tumour of breast, phyllodes tumour of the breast
Also known as:
PBS, breast sarcoma, sarcoma of breast, sarcoma of the breast
Also known as:
breast synovial sarcoma (disease)
Also known as:
BRCA1 hereditary breast ovarian cancer syndrome, BROVCA1, breast cancer, familial, susceptibility to, 1, breast-ovarian cancer, familial, 1, multifactorial, breast-ovarian cancer, familial, susceptibility to, 1, breast-ovarian cancer, familial, susceptibility to, type 1, hereditary breast ovarian cancer syndrome caused by mutation in BRCA1, ovarian cancer, familial, susceptibility to, 1, susceptibility to familial breast-ovarian cancer 1
Also known as:
BNAH1, amastia, amazia, athelia, breasts and/or nipples, aplasia or hypoplasia of, 1
Also known as:
BNAH2, PTPRF isolated congenital breast hypoplasia/aplasia, breasts and/or nipples, aplasia or hypoplasia of, 2, breasts and/or nipples, aplasia or hypoplasia of, type 2, isolated congenital breast hypoplasia/aplasia caused by mutation in PTPRF
Also known as:
Brill Zinsser disease, Brill disease, Brill's disease, latent typhus, recrudescent typhus, sporadic typhus
Also known as:
BCS1, EDS VIB (formerly), Ehlers-Danlos syndrome type 6B (formerly), Ehlers-Danlos syndrome type 6b, brittle cornea syndrome, brittle cornea syndrome 1, brittle cornea syndrome 2, brittle cornea syndrome type 1, kyphoscoliosis type, type VIB Ehlers-Danlos syndrome
Also known as:
BCS1, Ehlers-Danlos syndrome, type Vib, Ehlers-Danlos syndrome, type Vib, formerly, Fragilitas oculi with Joint hyperextensibility, ZNF469 brittle cornea syndrome, brittle cornea syndrome 1, brittle cornea syndrome caused by mutation in ZNF469, corneal fragility, keratoglobus, blue sclerae, Joint hyperextensibility, dysgenesis Mesodermalis corneae Et sclerae
Also known as:
BCS2, PRDM5 brittle cornea syndrome, brittle cornea syndrome 2, brittle cornea syndrome caused by mutation in PRDM5, brittle cornea syndrome type 2