Disease Index
9,486 diseasesfallopian tube benign neoplasm
Human disease
fallopian tube cancer
female reproductive organ cancer that is located in fallopian tube
fallot complex - intellectual disability - growth delay
Fallot complex - intellectual deficit - growth delay is a rare disorder characterized by tetralogy of Fallot, minor facial anomalies, and severe intellectual deficiency and growth delay
ICD: Q87.8MeSH: C536608
familial abdominal aortic aneurysm
Human disease
familial acute necrotizing encephalopathy
Familial acute necrotizing encephalopathy or ADANE is a potentially fatal neurological disease characterised by neuropathological lesions principally involving the brainstem, thalamus and putamen
familial adenomatous polyposis
autosomal dominant disease that is has material basis in mutations in the APC gene and involves formation of numerous polyps in the epithelium of the large intestine which are initially benign and later transform into colon cancer
ICD: C18MeSH: D011125
familial adenomatous polyposis 2
familial adenomatous polyposis that has material basis in homozygous or compound heterozygous mutation in the MUTYH gene on chromosome 1p34
familial adenomatous polyposis due to 5q22.2 microdeletion
human disease
familial adrenal hypoplasia with absent pituitary luteinizing hormone
human disease
MeSH: C565976
familial Alzheimer-like prion disease
hereditary prion disease with dementia
Familial amyloid cardiomyopathy
Transthyretin (TTR)-related familial amyloidotic cardiomyopathy is a hereditary TTR-related systemic amyloidosis (ATTR) with predominant cardiac involvement resulting from myocardial infiltration of abnormal amyloid protein
familial anetoderma
Familial anetoderma is an extremely rare genetic skin disease characterized by loss of elastin tissue leading to localized areas of flaccid skin and a family history of the disorder
familial angiolipomatosis
human disease
MeSH: C565951
Familial aortic dissection
medical condition
familial apolipoprotein C-II deficiency
human disease
familial articular hypermobility syndrome
familial atrial fibrillation
atrial fibrillation that has material basis in autosomal dominant inheritance of the familial atrial fibrillation (ATFB) genes
MeSH: C563817
familial atypical multiple mole melanoma syndrome
50) and a family history of melanoma as well as, in a subset of patients, an increased risk of developing pancreatic cancer (see this term) and other malignancies
familial benign flecked retina
human disease
MeSH: C565564
familial bicuspid aortic valve
human disease
Familial British dementia
medical condition
MeSH: C538208
familial calcium pyrophosphate deposition
MeSH: C563162
familial caudal dysgenesis
MeSH: C535879
familial cavitary optic disc anomaly
human disease
familial cervical artery dissection
instance of cervical artery dissection that is caused by an inherited modification of the individual's genome
familial chilblain lupus
instance of Chilblain lupus that is caused by an inherited modification of the individual's genome
familial chylomicronemia syndrome
human disease
Familial cirrhosis
congenital disorder of digestive system
MeSH: C566123
familial clubfoot due to 17q23.1q23.2 microduplication
17q23.1-q23.2 microduplication is a newly described cause of familial isolated clubfoot.
familial clubfoot due to 5q31 microdeletion
human disease