Phenotypes for disease #00146 (MATINS;MHA;BDPLT6 (macrothrombocytopenia, granulocyte inclusions with/without nephritis or sensorineural hearing loss (MATINS, May-Hegglin anomaly (MHA), bleeding disorder platelet type 6 (BDPLT-6))), OMIM:155100)

36 entries on 1 page. Showing entries 1 - 36.
Legend   How to query  

AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Protein     

Owner     

Individual ID     
0000174830 macrothrombocytopenia Familial, autosomal dominant 52y MATINS - - - platelet count 30x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), normal bleeding time (-HP:0003010), no bleeding diathesis (-HP:0001892), no proteinuria (-HP:0000093), no renal failure (-HP:0000083), bilateral sensorineural hearing loss (HP:0008619), no cataract (-HP:0000518) - Johan den Dunnen 00234419
0000174831 macrothrombocytopenia Familial, autosomal dominant 59y MATINS - - - platelet count 40x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), normal bleeding time (-HP:0003010), no bleeding diathesis (-HP:0001892), no proteinuria (-HP:0000093), no renal failure (-HP:0000083), bilateral sensorineural hearing loss (HP:0008619), bilateral cataract (HP:0000518) - Johan den Dunnen 00234420
0000174832 macrothrombocytopenia Familial, autosomal dominant 11y MATINS - - - platelet count 72x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), normal bleeding time (-HP:0003010), no bleeding diathesis (-HP:0001892), no proteinuria (-HP:0000093), no renal failure (-HP:0000083), no sensorineural hearing loss (-HP:0000407), no cataract (-HP:0000518) - Johan den Dunnen 00234421
0000174833 macrothrombocytopenia Unknown 25y MATINS - - - platelet count 25x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), increased bleeding time (HP:0003010), easy bruising, epistaxis, bleeding after teeth extraction, proteinuria (HP:0000093), no renal failure (-HP:0000083), bilateral sensorineural hearing loss (HP:0008619), no cataract (-HP:0000518) - Johan den Dunnen 00234422
0000174834 macrothrombocytopenia Familial, autosomal dominant 33y MATINS - - - platelet count 85x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), easy bruising, menorrhagia, epistaxis, no proteinuria (-HP:0000093), no renal failure (-HP:0000083), no sensorineural hearing loss (-HP:0000407), no cataract (-HP:0000518) - Johan den Dunnen 00234423
0000174836 macrothrombocytopenia Familial, autosomal dominant 02y MATINS - - - platelet count 96x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), no bleeding diathesis (-HP:0001892), no proteinuria (-HP:0000093), no renal failure (-HP:0000083), no sensorineural hearing loss (-HP:0000407) - Johan den Dunnen 00234424
0000174837 macrothrombocytopenia Familial, autosomal dominant 43y MATINS - - - platelet count 116x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), increased bleeding time (HP:0003010), easy bruising, gum bleeding, no proteinuria (-HP:0000093), no renal failure (-HP:0000083), no sensorineural hearing loss (-HP:0000407), no cataract (-HP:0000518) - Johan den Dunnen 00234425
0000174838 macrothrombocytopenia Familial, autosomal dominant 08y MATINS - - - platelet count 123x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), increased bleeding time (HP:0003010), epistaxis, bleeding after surgery and loss milk tooth, no proteinuria (-HP:0000093), no renal failure (-HP:0000083), no sensorineural hearing loss (-HP:0000407), no cataract (-HP:0000518) - Johan den Dunnen 00234426
0000174839 macrothrombocytopenia Unknown 20y MATINS - - - platelet count 65x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), easy bruising, epistaxis, no proteinuria (-HP:0000093), no renal failure (-HP:0000083), no sensorineural hearing loss (-HP:0000407), no cataract (-HP:0000518) - Johan den Dunnen 00234427
0000174841 macrothrombocytopenia Isolated (sporadic) - MATINS - - - see paper; ..., abnormal platelet function, granulocytes and megakaryocytes (not platelets) with inclusions - Johan den Dunnen 00234432
0000174842 macrothrombocytopenia Unknown 28y MATINS - - - see paper; ..., thrombocytopenia discovered by chance during check-up, no unusual susceptibility to bleeding, diagnosed with immune thrombocytopenic purpura - Johan den Dunnen 00234434
0000174843 macrothrombocytopenia Unknown 18y MATINS - - - see paper; ..., thrombocytopenia, mild mucocutaneous bleeding - Johan den Dunnen 00234433
0000174845 Fechtner syndrome Isolated (sporadic) - MATINS - - - see paper; … - Johan den Dunnen 00234436
0000174846 Fechtner syndrome Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234437
0000174847 Fechtner syndrome Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234438
0000174848 Fechtner syndrome Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234439
0000174849 Fechtner syndrome Isolated (sporadic) - MATINS - - - see paper; … - Johan den Dunnen 00234440
0000174850 Epstein syndrome Isolated (sporadic) - MATINS - - - see paper; … - Johan den Dunnen 00234441
0000174851 Epstein syndrome Isolated (sporadic) - MATINS - - - see paper; … - Johan den Dunnen 00234442
0000174852 Epstein syndrome Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234443
0000174853 Epstein syndrome Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234444
0000174854 Epstein syndrome Isolated (sporadic) - MATINS - - - see paper; … - Johan den Dunnen 00234445
0000174855 May-Hegglin anamoly/Sebastian syndrome Isolated (sporadic) - MATINS - - - see paper; … - Johan den Dunnen 00234446
0000174856 May-Hegglin anamoly Isolated (sporadic) - MATINS - - - see paper; … - Johan den Dunnen 00234447
0000174857 May-Hegglin anamoly/Sebastian syndrome Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234448
0000174858 May-Hegglin anamoly/Sebastian syndrome Isolated (sporadic) - MATINS - - - see paper; … - Johan den Dunnen 00234449
0000174859 May-Hegglin anamoly Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234450
0000174860 May-Hegglin anamoly/Sebastian syndrome Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234451
0000174861 May-Hegglin anamoly Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234452
0000174862 May-Hegglin anamoly Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234453
0000174863 May-Hegglin anamoly Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234454
0000174866 May-Hegglin anamoly Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234457
0000174867 Sebastian syndrome Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234458
0000174868 Sebastian syndrome Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234459
0000174869 Fechtner syndrome Familial, autosomal dominant - MATINS - - - see paper; … - Johan den Dunnen 00234460
0000174870 Fechtner syndrome Isolated (sporadic) - MATINS - - - see paper; … - Johan den Dunnen 00234461
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.