Also known as:
HPC, Hp, PCTT, autosomal dominant hereditary pancreatitis, familial pancreatitis, hereditary chronic pancreatitis, hereditary pancreatitis, pancreatitis, calcific, pancreatitis, calcific, included, pancreatitis, chronic, pancreatitis, chronic pancreatitis, chronic, susceptibility to, included, pancreatitis, chronic, protection against, pancreatitis, chronic, protection against, included, pancreatitis, chronic, susceptibility to, pancreatitis, hereditary
Also known as:
Hereditary clear cell renal cell cancer, hereditary clear cell renal carcinoma, hereditary clear cell renal cell adenocarcinoma, hereditary clear cell renal cell carcinoma, hereditary conventional (clear cell) renal cell carcinoma, hereditary conventional renal cell carcinoma
Also known as:
continuous muscle fiber activity hereditary, continuous muscle fibre activity hereditary
Also known as:
ChC type 2, GLUT1 deficiency syndrome with pseudohyperkalemia and hemolysis, SDCHCN, cryohydrocytosis, stomatin-deficient, with intellectual disability, seizures, cataracts, and massive hepatosplenomegaly, cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly, hereditary cryohydrocytosis type 2, sdCHC, stomatin-deficient cryohydrocytosis, stomatin-deficient cryohydrocytosis with neurologic defects
Also known as:
FDGC, HDGC, diffuse gastric cancer, familial diffuse cancer of stomach, familial diffuse gastric cancer, hereditary diffuse cancer of stomach, hereditary diffuse gastric adenocarcinoma, hereditary diffuse gastric cancer, signet cell adenocarcinoma, signet ring cell gastric carcinoma, signet ring gastric carcinoma
Also known as:
Isaacs syndrome, ea syndrome, episodic ataxia, episodic ataxia syndrome
Also known as:
congenital defect of folate absorption, congenital folate malabsorption, folate malabsorption, hereditary, folic acid transport defect
