Phenotypes for disease #01575 (HHT (telangiectasia hemorrhagic, hereditary (HHT)))

71 entries on 1 page. Showing entries 1 - 71.
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Phenotype/Onset     

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Individual ID     
0000053401 hereditary hemorrhagic telangiectasia with frequent epistaxis at 12y - - Unknown - - - - - Sophie Nambot 00038520
0000053403 hereditary hemorrhagic telangiectasia with recurrent but sporadic epistaxis - - Unknown - - - - - Sophie Nambot 00038516
0000078715 - - - Unknown - - - - - Gemeinschaftspraxis für Humangenetik Dresden 00100507
0000078717 suspected Morbus Osler - - Familial, autosomal dominant - - - - - Andreas Laner 00035680
0000078718 suspected Morbus Osler with epistaxis (also familiar), intracranial haemorrhage with 4 arteriovenous malformations - - Familial, autosomal dominant - - - - - Andreas Laner 00035681
0000078719 - - - Familial, autosomal dominant - - - - - Andreas Laner 00035682
0000078720 suspected Morbus Osler - - Familial, autosomal dominant - - - - - Andreas Laner 00035683
0000078721 clinical Morbus Osler - - Familial, autosomal dominant - - - - - Andreas Laner 00035687
0000078722 suspected Morbus Osler - - Familial, autosomal dominant - - - - - Andreas Laner 00035685
0000078723 suspected Morbus Osler with epistaxis (also familiar), intracranial haemorrhage with 4 arteriovenous malformations - - Familial, autosomal dominant - - - - - Andreas Laner 00035684
0000078724 suspected Morbus Osler - - Familial, autosomal dominant - - - - - Andreas Laner 00035689
0000155273 epistaxis, pulmonary arteriovenous malformation, hepatic arteriovenous malformation hereditary haemorrhagict elangiectasia HHT-2 Familial, autosomal dominant 63y - - - - Johan den Dunnen 00207450
0000155280 epistaxis, telangiectasia, pulmonary arteriovenous malformation hereditary haemorrhagict elangiectasia HHT-2 Familial, autosomal dominant 27y - - - - Johan den Dunnen 00207502
0000155281 epistaxis, telangiectasia, pulmonary arteriovenous malformation hereditary haemorrhagict elangiectasia HHT-2 Unknown 41y - - - - Johan den Dunnen 00207503
0000155282 epistaxis, telangiectasia, colon arteriovenous malformation hereditary haemorrhagict elangiectasia HHT-2 Familial, autosomal dominant 64y - - - - Johan den Dunnen 00207504
0000155283 epistaxis, telangiectasia, pulmonary arteriovenous malformation, hepatic arteriovenous malformation hereditary haemorrhagict elangiectasia HHT-2 Familial, autosomal dominant 47y - - - - Johan den Dunnen 00207505
0000155284 telangiectasia, pulmonary arteriovenous malformation, hepatic arteriovenous malformation hereditary haemorrhagict elangiectasia HHT-2 Familial, autosomal dominant 70y - - - - Johan den Dunnen 00207506
0000155285 epistaxis, diffuse arteriovenous malformation hereditary haemorrhagict elangiectasia HHT-2 Familial, autosomal dominant 49y - - - - Johan den Dunnen 00207507
0000155286 epistaxis, telangiectasia, pulmonary arteriovenous malformation hereditary haemorrhagict elangiectasia HHT-2 Familial, autosomal dominant 80y - - - - Johan den Dunnen 00207508
0000167202 JP-HHT - - Unknown - - - - - Karl Heinimann 00218666
0000167203 JP-HHT - - Unknown - - - - - Karl Heinimann 00218667
0000167206 JP-HHT - - Unknown - - - - - Karl Heinimann 00218670
0000167207 JP-HHT - - Unknown - - - - - Karl Heinimann 00218671
0000167208 JP-HHT - - Unknown - - - - - Karl Heinimann 00218672
0000167218 JP-HHT - - Unknown - - - - - Karl Heinimann 00218682
0000167219 JP-HHT - - Unknown - - - - - Karl Heinimann 00218683
0000167238 JP-HHT - - Unknown - - - - - Karl Heinimann 00218702
0000167239 JP-HHT - - Unknown - - - - - Karl Heinimann 00218703
0000167240 JP-HHT - - Unknown - - - - - Karl Heinimann 00218704
0000167241 JP-HHT - - Unknown - - - - - Karl Heinimann 00218705
0000167242 JP-HHT - - Unknown - - - - - Karl Heinimann 00218706
0000167258 JP-HHT - - Unknown - - - - - Karl Heinimann 00218722
0000167266 JP-HHT - - Unknown - - - - - Karl Heinimann 00218730
0000167267 JP-HHT - - Unknown - - - - - Karl Heinimann 00218731
0000167270 JP-HHT - - Unknown - - - - - Karl Heinimann 00218734
0000167311 JP-HHT - - Unknown - - - - - Karl Heinimann 00218775
0000167312 JP-HHT - - Unknown - - - - - Karl Heinimann 00218776
0000167314 JP-HHT - - Unknown - - - - - Karl Heinimann 00218778
0000167318 JP-HHT - - Unknown - - - - - Karl Heinimann 00218782
0000167346 JP-HHT - - Unknown - - - - - Karl Heinimann 00218810
0000167347 JP-HHT - - Unknown - - - - - Karl Heinimann 00218811
0000167349 JP-HHT - - Unknown - - - - - Karl Heinimann 00218813
0000167350 JP-HHT - - Unknown - - - - - Karl Heinimann 00218814
0000167357 JP-HHT - - Unknown - - - - - Karl Heinimann 00218821
0000167358 HHT - - Unknown - - - - - Karl Heinimann 00218822
0000167359 HHT - - Unknown - - - - - Karl Heinimann 00218823
0000167360 HHT - - Unknown - - - - - Karl Heinimann 00218824
0000167379 JP-HHT - - Unknown - - - - - Karl Heinimann 00218843
0000167380 JP-HHT - - Unknown - - - - - Karl Heinimann 00218844
0000167381 JP-HHT - - Unknown - - - - - Karl Heinimann 00218845
0000167382 JP-HHT - - Unknown - - - - - Karl Heinimann 00218846
0000167383 JP-HHT - - Unknown - - - - - Karl Heinimann 00218847
0000167385 JP-HHT - - Unknown - - - - - Karl Heinimann 00218849
0000167386 JP-HHT - - Unknown - - - - - Karl Heinimann 00218850
0000167387 JP-HHT - - Unknown - - - - - Karl Heinimann 00218851
0000167440 JP-HHT - - Unknown - - - - - Karl Heinimann 00218904
0000167441 JP-HHT - - Unknown - - - - - Karl Heinimann 00218905
0000167442 JP-HHT - - Unknown - - - - - Karl Heinimann 00218906
0000167443 JP-HHT - - Unknown - - - - - Karl Heinimann 00218907
0000167444 JP-HHT - - Unknown - - - - - Karl Heinimann 00218908
0000167445 JP-HHT - - Unknown - - - - - Karl Heinimann 00218909
0000167446 JP-HHT - - Unknown - - - - - Karl Heinimann 00218910
0000167447 JP-HHT - - Unknown - - - - - Karl Heinimann 00218911
0000207614 57y-deceased; recurrent epistaxis, telangiectasia; family history telangiectasia HHT-1 Familial, autosomal dominant 57y - - - - Johan den Dunnen 00269823
0000207615 recurrent epistaxis, telangiectasia, visceral arteriovenous malformation, liver arteriovenous malformation, chronic HHT-related GI bleeding; family history telangiectasia HHT-2 Familial, autosomal dominant 70y - - - - Johan den Dunnen 00269824
0000207616 recurrent epistaxis, telangiectasia, visceral arteriovenous malformation, liver arteriovenous malformation, chronic HHT-related GI bleeding; family history telangiectasia HHT-2 Familial, autosomal dominant 66y - - - - Johan den Dunnen 00269825
0000207617 recurrent epistaxis, telangiectasia; family history telangiectasia HHT-2 Familial, autosomal dominant 71y - - - - Johan den Dunnen 00269826
0000207618 recurrent epistaxis, telangiectasia, visceral arteriovenous malformation, liver arteriovenous malformation, chronic HHT-related GI bleeding; family history telangiectasia HHT-2 Familial, autosomal dominant 68y - - - - Johan den Dunnen 00269827
0000330504 see paper; ..., classical hereditary hemorrhagic telangiectasia, severe nosebleeds needing blood transfusion and intravenous iron hereditary hemorrhagic telangiectasia - Unknown - - - - - Johan den Dunnen 00440592
0000330505 see paper; ..., classical hereditary hemorrhagic telangiectasia, daily nosebleeds; one had pulmonary arteriovenous malformations requiring treatment, hemihypertrophy (left-right axis defect) hereditary hemorrhagic telangiectasia - Unknown - - - - - Johan den Dunnen 00440593
0000330506 see paper; ..., colonic and gastric polyposis, nosebleeds, mucocutaneous telangiectasia, pulmonary AVMs treated by embolization; JPHT family history hereditary hemorrhagic telangiectasia JPHT Familial, autosomal dominant - - - - - Johan den Dunnen 00440594
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