Familial, Familial hyperaldosteronism, Familial hypercholesterolemia, Familial hypocalciuric hypercalcemia, Familial amyloid neuropathy, Familial dysalbuminemic hyperthyroxinemia, Familial dysautonomia, Familial Mediterranean fever, Familial exudative vitreoretinopathy, Progressive familial intrahepatic cholestasis, Familial hypertriglyceridemia, Familial (album), Familial benign copper deficiency, Familial adenomatous polyposis, Benign familial neonatal seizures, Familial renal disease in animals, Familial hemiplegic migraine, Familial multiple lipomatosis, St. Helena familial genu valgum, Familial dysbetalipoproteinemia, Familial British dementia, Familial osteodysplasia, Anderson type, Benign familial infantile epilepsy, Familial disseminated comedones without dyskeratosis, Familial amyloid polyneuropathy, Familial multiple intestinal atresia, RUNX1 Familial Platelet Disorder, Normophosphatemic familial tumoral calcinosis, Familial encephalopathy with neuroserpin inclusion bodies, Familial eosinophilia, Primary familial brain calcification, Familial male-limited precocious puberty, Familial amyloid cardiomyopathy, Familial isolated vitamin E deficiency, Familial cutaneous collagenoma, Fatal insomnia, Familial nasal acilia, Lipoprotein lipase deficiency, Nine familial exterminations, Hailey–Hailey disease, Familial atrial fibrillation

Familial episodic pain syndrome, Familial sleep traits, Familial synovial chondromatosis with dwarfism, Familial cirrhosis, Attenuated familial adenomatous polyposis, Dunnigan familial partial lipodystrophy, Familial Danish dementia, Familial thoracic aortic aneurysm, Familial natural short sleep, Familial homicide, Vestibulocochlear dysfunction progressive familial, Familial Amyloidosis, Finnish Type, Antiphospholipid syndrome, familial, Early-onset Alzheimer's disease, Familial progressive hyperpigmentation, Gardner's syndrome, Dysplastic nevus syndrome, Familial thoracic aortic aneurysm and aortic dissection, Familial Alzheimer-like prion disease, Familial dwarfism and painful muscle spasms, Cooperative Escapism in Familial Relations, Cold urticaria, Familial renal amyloidosis, Familial aortic dissection, Paroxysmal nonkinesigenic dyskinesia, Hyperlipidemia, Familial partial lipodystrophy, Glucocorticoid deficiency 1, Hypobetalipoproteinemia, Familial multiple cafe-au-lait spots, European Registry of Hereditary Pancreatitis and Pancreatic Cancer, CYLD cutaneous syndrome, Combined hyperlipidemia, Camptodactyly-taurinuria syndrome, Lucey–Driscoll syndrome, Paroxysmal extreme pain disorder, Apolipoprotein B deficiency, Familialism, Familial opposable triphalangeal thumbs duplication, Family aggregation, Cerebral amyloid angiopathy, Periodic paralysis, Pseudohypoaldosteronism, Storge, Hereditary cancer syndrome, Advanced sleep phase disorder, Multiple minute digitate hyperkeratosis, Infantile convulsions and choreoathetosis, Renal glycosuria, Chronic mucocutaneous candidiasis

Familial, Familial hyperaldosteronism, Familial hypercholesterolemia, Familial hypocalciuric hypercalcemia, Familial amyloid neuropathy, Familial dysalbuminemic hyperthyroxinemia, Familial dysautonomia, Familial Mediterranean fever, Familial exudative vitreoretinopathy, Progressive familial intrahepatic cholestasis, Familial hypertriglyceridemia, Familial (album), Familial benign copper deficiency, Familial adenomatous polyposis, Benign familial neonatal seizures, Familial renal disease in animals, Familial hemiplegic migraine, Familial multiple lipomatosis, St. Helena familial genu valgum, Familial dysbetalipoproteinemia, Familial British dementia, Familial osteodysplasia, Anderson type, Benign familial infantile epilepsy, Familial disseminated comedones without dyskeratosis, Familial amyloid polyneuropathy, Familial multiple intestinal atresia, RUNX1 Familial Platelet Disorder, Normophosphatemic familial tumoral calcinosis, Familial encephalopathy with neuroserpin inclusion bodies, Familial eosinophilia, Primary familial brain calcification, Familial male-limited precocious puberty, Familial amyloid cardiomyopathy, Familial isolated vitamin E deficiency, Familial cutaneous collagenoma, Fatal insomnia, Familial nasal acilia, Lipoprotein lipase deficiency, Nine familial exterminations, Hailey–Hailey disease, Familial atrial fibrillation, Familial episodic pain syndrome, Familial sleep traits, Familial synovial chondromatosis with dwarfism, Familial cirrhosis, Attenuated familial adenomatous polyposis, Dunnigan familial partial lipodystrophy, Familial Danish dementia, Familial thoracic aortic aneurysm, Familial natural short sleep, Familial homicide, Vestibulocochlear dysfunction progressive familial, Familial Amyloidosis, Finnish Type, Antiphospholipid syndrome, familial, Early-onset Alzheimer's disease, Familial progressive hyperpigmentation, Gardner's syndrome, Dysplastic nevus syndrome, Familial thoracic aortic aneurysm and aortic dissection, Familial Alzheimer-like prion disease, Familial dwarfism and painful muscle spasms, Cooperative Escapism in Familial Relations, Cold urticaria, Familial renal amyloidosis, Familial aortic dissection, Paroxysmal nonkinesigenic dyskinesia, Hyperlipidemia, Familial partial lipodystrophy, Glucocorticoid deficiency 1, Hypobetalipoproteinemia, Familial multiple cafe-au-lait spots, European Registry of Hereditary Pancreatitis and Pancreatic Cancer, CYLD cutaneous syndrome, Combined hyperlipidemia, Camptodactyly-taurinuria syndrome, Lucey–Driscoll syndrome, Paroxysmal extreme pain disorder, Apolipoprotein B deficiency, Familialism, Familial opposable triphalangeal thumbs duplication, Family aggregation, Cerebral amyloid angiopathy, Periodic paralysis, Pseudohypoaldosteronism, Storge, Hereditary cancer syndrome, Advanced sleep phase disorder, Multiple minute digitate hyperkeratosis, Infantile convulsions and choreoathetosis, Renal glycosuria, Chronic mucocutaneous candidiasis, Multiple endocrine neoplasia, Iminoglycinuria, Hypokalemic periodic paralysis, Hyperaldosteronism, Caisse d'allocations familiales, Hemophagocytic lymphohistiocytosis, Benign hereditary chorea, Hyperproinsulinemia, Hereditary nonpolyposis colorectal cancer, PAPA syndrome, Isolated growth hormone deficiency, Upington disease, Thin basement membrane disease, Microvillous inclusion disease, Hereditary sensory and autonomic neuropathy, Hypertryptophanemia, Family values, DNA profiling, Dihydropyrimidine dehydrogenase deficiency, Tangier disease, Porphyria cutanea tarda, Cavernous hemangioma, Anetoderma, Cherubism, Megaduodenum, Essential hypertension, Polycythemia, Gilbert's syndrome, Pituitary adenoma, Hypouricemia, Dysfibrinogenemia, Aromatase excess syndrome, Howel–Evans syndrome, Primary hyperparathyroidism, Shar Pei, X-linked reticulate pigmentary disorder, Cardiac myxoma, Abetalipoproteinemia, Prolactinoma, Amyloidosis, Actinic prurigo, CDKN2A, Calcium pyrophosphate dihydrate crystal deposition disease, Amyloid, Family estrangement, Hemolytic–uremic syndrome, Arrhythmogenic cardiomyopathy, Fanconi syndrome, Progressive myoclonus epilepsy, Peeling skin syndrome, Birt–Hogg–Dubé syndrome, Medullary thyroid cancer, Hypertrophic cardiomyopathy, Essential tremor, Renal–hepatic–pancreatic dysplasia, ALS, Dilated cardiomyopathy, Gitelman syndrome, Hereditary spastic paraplegia, Mitral valve prolapse