Encyclopedia results for familial

1. Familial love
   
   Love table In sociology , familial love is a type affinity or natural affection felt between members of a group bound by common ancestry or blood ties, or through friendship and care. Familial love can ..
   
   
   
   
2. Familial homicide
   
   Orphan date September 2008 Familial homicide is a form of homicide that is illegal by the United Kingdom ... CJS on familial homicide http news.bbc.co.uk 1 hi wales south west 6181051.stm Mother jailed after ..
   
   
   
   
3. Familial dysautonomia
   
   DiseaseDisorder infobox Name Familial dysautonomia Image Riley day.jpg Caption Facial features of a patient with familial dysautonomia over time. Note flattening of upper lip. By age 10 years prominence ..
   
   
   
   
4. Familial hypercholesterolemia
   
   DiseaseDisorder infobox Name Familial hypercholesterolemia Image Caption ICD10 ICD10 E 78 0 e 70 ICD9 ... MeshID D006938 Familial hypercholesterolemia abbreviated FH , also spelled familial hypercholesterolaemia ..
   
   
   
   
5. Familial cold autoinflammatory syndrome
   
   Infobox Disease Name PAGENAME Image Caption DiseasesDB ICD10 ICD9 ICDO OMIM 120100 MedlinePlus eMedicineSubj eMedicineTopic MeshID Familial cold autoinflammatory syndrome is a syndrome Mendelian Inher ...
   
   
   
   
6. Familial amyloid neuropathy
   
   MedlinePlus eMedicineSubj eMedicineTopic MeshID D028227 The familial amyloid neuropathies or familial amyloidotic neuropathies , neuropathic heredofamilial amyloidosis , familial amyloid polyneuropathy ..
   
   
   
   
7. Familial thoracic aortic aneurysm
   
   MedlinePlus eMedicineSubj emerg eMedicineTopic 28 MeshID Familial thoracic aortic aneurysm also referred to as familial aortic dissection or cystic medial necrosis of aorta ref name omim OMIM 607086 ref ..
   
   
   
   
8. Familial atrial fibrillation
   
   ICDO OMIM 608583 MedlinePlus eMedicineSubj eMedicineTopic MeshID Familial atrial fibrillation is an autosomal ... and sudden death. Complications of familial atrial fibrillation can occur at any age, although ..
   
   
   
   
9. Familial amyloid polyneuropathy
   
   Familial amyloid polyneuropathy FAP or Corino de Andrade s disease , a form of Paramyloidosis , is a neurodegenerative .... It is a fatal and incurable disease. Cause Image Autodominant.jpg thumb right Familial ..
   
   
   
   
10. Familial hemiplegic migraine
    
    219 Familial hemiplegic migraine FHM is an autosomal dominant classical migraine subtype ... familial infantile convulsion s, and alternating hemiplegia of childhood . There are 3 known Locus ..
    
    
    
    
11. Familial renal disease in animals
    
    Familial renal disease in animals is an uncommon cause of renal failure kidney failure in young dog s and cat s. Most causes are breed related familial and some are inherited. Some are congenital disorder ..
    
    
    
    
12. Fatal familial insomnia
    
    ICDO OMIM 600072 MedlinePlus eMedicineSubj eMedicineTopic MeshID D034062 Fatal familial insomnia FFI ... fatal. History Fatal familial insomnia was first detected by Italian doctor Ignazio Roiter in 1974 ..
    
    
    
    
13. Familial renal amyloidosis
    
    ICDO OMIM 105200 MedlinePlus eMedicineSubj med eMedicineTopic 3379 MeshID Familial renal amyloidosis or familial visceral amyloidosis , or hereditary amyloid nephropathy is a form of amyloidosis primarily ..
    
    
    
    
14. Familial Mediterranean fever
    
    Infobox Disease Name Familial Mediterranean fever Image Caption DiseasesDB 9836 ICD10 ICD10 E 85 0 e ... 1410 MeshID D010505 Familial Mediterranean fever FMF is a genetic disorder hereditary inflammation ..
    
    
    
    
15. Progressive familial intrahepatic cholestasis
    
    601847 OMIM2 602347 MedlinePlus eMedicineSubj ped eMedicineTopic 2771 MeshID Progressive familial intrahepatic cholestasis PFIC refers to a group of familial cholestasis cholestatic conditions caused ..
    
    
    
    
16. Benign familial neonatal convulsions
    
    Infobox Disease Name Benign familial neonatal convulsions Image Caption DiseasesDB 33689 ICD10 ICD10 ... eMedicineTopic 32 MeshID D020936 Benign familial neonatal convulsions BFNC is a rare autosomal dominant ..
    
    
    
    
17. Familial adenomatous polyposis
    
    with familial adenomatous polyposis. DiseasesDB 4678 ICD10 ICD10 C 18 c 15 , ICD10 D 12 d 10 ... Familial adenomatous polyposis FAP is an inherited condition in which numerous Polyp medicine polyp ..
    
    
    
    
18. Familial cutaneous papillomatosis
    
    refimprove date January 2008 Infobox Disease Name PAGENAME Image Caption DiseasesDB ICD10 ICD9 ICDO OMIM 167900 MedlinePlus eMedicineSubj eMedicineTopic MeshID Familial cutaneous papillomatosis , also ...
    
    
    
    
19. Danubian endemic familial nephropathy
    
    Infobox Disease Name PAGENAME Image Caption DiseasesDB 31409 ICD10 ICD10 N 15 0 n 10 ICD9 ICDO OMIM 124100 MedlinePlus eMedicineSubj eMedicineTopic MeshID D001449 Danubian endemic familial nephropathy ...
    
    
    
    
20. Familial isolated vitamin e deficiency
    
    OMIM mult OMIM2 600415 MedlinePlus eMedicineSubj eMedicineTopic MeshID Familial Isolated Vitamin ... of Friedreich ataxia . Cause Familial Isolated Vitamin E Deficiency is caused by mutations in the gene ..
    
    
    
    
21. Familial encephalopathy with neuroserpin inclusion bodies
    
    Familial encephalopathy with neuroserpin inclusion bodies FENIB is a progressive disorder of the nervous ... care. The signs and symptoms of familial encephalopathy with neuroserpin inclusion bodies ..
    
    
    
    
22. Hailey Hailey Disease (Familial Benign Pemphigus)
    
    ICDO OMIM 169600 MedlinePlus eMedicineSubj eMedicineTopic MeshID D016506 Familial benign pemphigus ..., H. Hailey. Familial benign chronic pemphigus. Report of 13 cases in four generations of a family and report ..
    
    
    
    
23. Familial dysfibrinogenemia
    
    unreferenced date October 2007 The dysfibrinogenemias are a group of autosomal dominant disorders of qualitatively abnormal fibrinogen s. There are various different fibrinogen abnormalities, each nam ...
    
    
    
    
24. FCAS
    
    FCAS may refer to Familial Cold Autoinflammatory Syndrome , a genetic disease Fixed Content Aware Storage , an industry trade group disambiguation ..
    
    
    
    
25. ARH
    
    ARH may refer to Armed Reconnaissance Helicopter Familial hypercholesterolemia Autosomal recessive hypercholesterolemia The LDLRAP1 ARH gene disambig de ARH fr ARH it ARH ..
    
    
    
    

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