Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

13 matching diseasesClear search ×

Familial pancreatic carcinoma

Familial pancreatic cancer

ORPHA:1333

Familial atypical multiple mole melanoma syndrome

B-K mole syndrome · FAMM-PC syndrome

ORPHA:404560

Familial calcium pyrophosphate deposition

Calcium pyrophosphate dihydrate crystal deposition disease · Familial CC

ORPHA:1416

Familial colorectal cancer Type X

FCCTX

ORPHA:440437

Familial prostate cancer

ORPHA:1331

Hereditary breast cancer

Familial breast cancer · Familial breast carcinoma

ORPHA:227535

Hereditary diffuse gastric cancer

FDGC · Familial diffuse cancer of stomach

ORPHA:26106

Hereditary nonpolyposis colon cancer

Familial nonpolyposis colon cancer · Familial nonpolyposis colorectal cancer

ORPHA:443909

Neuroendocrine carcinoma of pancreas

Pancreatic NEC · Pancreatic neuroendocrine carcinoma

ORPHA:506098

Neuroendocrine neoplasm of pancreas

Pancreatic neuroendocrine neoplasm · Pancreatic NEN

ORPHA:506052

Neuroendocrine tumor of pancreas

Well-differentiated pancreatic neuroendocrine neoplasm · Well-differentiated NEN of pancreas

ORPHA:97253

OBSOLETE: Familial ovarian cancer

OBSOLETE: Familial ovarian malignant tumor

ORPHA:213517

VIPoma

Diarrheogenic islet cell tumor · Pancreatic cholera

ORPHA:97282