Phenotypes for disease #02210 (ATS1 (Alport syndrome, type 1, X-linked), OMIM:301050)

140 entries on 2 pages. Showing entries 1 - 100.
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0000060480 Alport syndrome (OMIM:301050) - - Familial, X-linked - - - - - Daniel Trujillano 00080911
0000071786 micro and macro haematuria, proteinuria; 21y renal failure; hearing loss; renal failure - - Familial, X-linked - - - - - Judy Savige 00093395
0000071787 Age at study 34y microscopic haematuria, proteinuria.; hearing loss; glomerulus abnormal - - Familial, X-linked - - - - - Judy Savige 00093396
0000071788 17y renal failure; microscopic haematuria, nephrotic syndrome, FSGS; renal failure - - Familial, X-linked - - - - - Judy Savige 00093397
0000071789 Age at study 15y microscopic haematuria, proteinuria, MPG - - Familial, X-linked - - - - - Judy Savige 00093398
0000071790 Age at study 5y micro and macro haematuria, proteinuria, MCD; no hearing loss; no ocular phenotype - - Familial, X-linked - - - - - Judy Savige 00093399
0000071791 Age at study7y microscopic haematuria, proteinuria, MPG; no hearing loss; no ocular phenotype - - Familial, X-linked - - - - - Judy Savige 00093400
0000071792 Age at study 9y micro and macro haematuria, proteinuria, MCD; hearing loss; no ocular phenotype; glomerulus abnormal - - Familial, X-linked - - - - - Judy Savige 00093401
0000071793 14y renal failure; microscopic haematuria, proteinuria, MPG; hearing loss; renal failure - - Familial, X-linked - - - - - Judy Savige 00093402
0000071794 Age at study 5y microscopic haematuria, proteinuria, MCD; no hearing loss; no ocular phenotype; glomerulus abnormal - - Familial, X-linked - - - - - Judy Savige 00093403
0000071795 Age at study 28y microscopic haematuria, proteinuria, FSGS; hearing loss; glomerulus abnormal - - Familial, X-linked - - - - - Judy Savige 00093404
0000071796 age at study 17y micro and macro haematuria, nephrotic syndrome, MPG; hearing loss - - Familial, X-linked - - - - - Judy Savige 00093405
0000071797 Age at study 9y microscopic haematuria - - Familial, X-linked - - - - - Judy Savige 00093406
0000071798 Age at study 17y microcopic haematuria, FSGS - - Familial, X-linked - - - - - Judy Savige 00093407
0000071799 25y renal failure; microscopic haematuria, nephrotic syndrome, FSGS; hearing loss; no ocular phenotype; renal failure - - Familial, X-linked - - - - - Judy Savige 00093408
0000071800 Age at study 21ymicroscopic haematuria, proteinuria, FSGS; no hearing loss; glomerulus abnormal - - Familial, X-linked - - - - - Judy Savige 00093409
0000071801 Age at study 20y microscopic haematuria, nephrotic syndrome; no hearing loss; ocular changes - - Familial, X-linked - - - - - Judy Savige 00093410
0000071802 Age at study 5y microscopic haematuria, proteinuria, MCD - - Familial, X-linked - - - - - Judy Savige 00093411
0000071803 Age at study 20y microscopic haematuria, proteinuria; no hearing loss; no ocular phenotype - - Familial, X-linked - - - - - Judy Savige 00093412
0000071804 Age at study 45y microscopic haematuria, proteinuria; no hearing loss - - Familial, X-linked - - - - - Judy Savige 00093413
0000071805 Age at study 24y microscopic haematuria, nephrotic syndrome, FSGS; hearing loss; no ocular phenotype - - Familial, X-linked - - - - - Judy Savige 00093414
0000071806 31y renal failure; microscopic haematuria, nephrotic syndrome; hearing loss; no ocular phenotype; renal failure - - Familial, X-linked - - - - - Judy Savige 00093415
0000071807 Age at study 8y micro and macro haematuria, proteinuria - - Familial, X-linked - - - - - Judy Savige 00093416
0000071808 Age at study 22y microscopic haematuria, nephrotic syndrome, FSGS; no hearing loss; no ocular phenotype; glomerulus abnormal - - Familial, X-linked - - - - - Judy Savige 00093417
0000071809 30y renal failure; microscopic haematuria, proteinuria, FSGS; hearing loss; ocular changes; renal failure - - Familial, X-linked - - - - - Judy Savige 00093418
0000071810 22y renal failure; microscopic haematuria, nephrotic syndrome, FSGS; no hearing loss; renal failure - - Familial, X-linked - - - - - Judy Savige 00093419
0000071811 Age at study 37y microscopic haematuria, nephrotic syndrome, FSGS; hearing loss; ocular changes - - Familial, X-linked - - - - - Judy Savige 00093420
0000071812 Age at study 7y microscopic haematuria, proteinuria - - Familial, X-linked - - - - - Judy Savige 00093421
0000071813 - - - Familial, X-linked - - - - - Judy Savige 00093422
0000071814 - - - Familial, X-linked - - - - - Judy Savige 00093423
0000071815 - - - Familial, X-linked - - - - - Judy Savige 00093424
0000071816 - - - Familial, X-linked - - - - - Judy Savige 00093425
0000071817 - - - Familial, X-linked - - - - - Judy Savige 00093426
0000071818 - - - Familial, X-linked - - - - - Judy Savige 00093427
0000071819 - - - Familial, X-linked - - - - - Judy Savige 00093428
0000071820 - - - Familial, X-linked - - - - - Judy Savige 00093429
0000071821 - - - Familial, X-linked - - - - - Judy Savige 00093430
0000071822 - - - Familial, X-linked - - - - - Judy Savige 00093431
0000071823 - - - Familial, X-linked - - - - - Judy Savige 00093432
0000071824 - - - Familial, X-linked - - - - - Judy Savige 00093433
0000071825 - - - Familial, X-linked - - - - - Judy Savige 00093434
0000071826 - - - Familial, X-linked - - - - - Judy Savige 00093435
0000071827 - - - Familial, X-linked - - - - - Judy Savige 00093436
0000071828 - - - Familial, X-linked - - - - - Judy Savige 00093437
0000071829 - - - Familial, X-linked - - - - - Judy Savige 00093438
0000071830 - - - Familial, X-linked - - - - - Judy Savige 00093439
0000071845 Alports, klinefelter syndromes and craniopharyngioma - - Familial, X-linked - - - - - Judy Savige 00093454
0000071846 haematuria and proteinuria at 3y, GBM abnormalities at 7, heavy proteinuria and hypoalbuminemia, and normal renal function. ; no ocular phenotype; glomerulus normal - - Familial, X-linked - - - - - Judy Savige 00093455
0000071847 - - - Familial, X-linked - - - - - Judy Savige 00093456
0000071848 - - - Familial, X-linked - - - - - Judy Savige 00093457
0000071849 - - - Familial, X-linked - - - - - Judy Savige 00093458
0000072356 18y renal failure; hearing loss; ocular changes; renal failure, lomerulus abnormal - - Familial, X-linked - - - - - Maria João Nabais Sá 00093965
0000072357 28y renal failure; hearing loss; ocular changes; renal failure, lomerulus abnormal - - Familial, X-linked - - - - - Maria João Nabais Sá 00093966
0000072358 21y renal failure; hearing loss; ocular changes; renal failure, lomerulus abnormal - - Familial, X-linked - - - - - Maria João Nabais Sá 00093967
0000072359 45y renal failure; hearing loss; no ocular phenotype; renal failure, lomerulus abnormal - - Familial, X-linked - - - - - Maria João Nabais Sá 00093968
0000072360 28y renal failure; hearing loss; no ocular phenotype; renal failure - - Familial, X-linked - - - - - Maria João Nabais Sá 00093969
0000072361 22y renal failure; hearing loss; renal failure - - Familial, X-linked - - - - - Maria João Nabais Sá 00093970
0000072362 hearing loss; no ocular phenotype; no renal failure, glomerulus abnormal - - Familial, X-linked - - - - - Maria João Nabais Sá 00093971
0000072364 20y renal failure; hearing loss; renal failure - - Familial, X-linked - - - - - Maria João Nabais Sá 00093973
0000072365 History of microscopic hematuria, proteinuria and CKD stage 3; no hearing loss; no renal failure - - Familial, X-linked - - - - - Maria João Nabais Sá 00093974
0000072366 17y renal failure; hearing loss; renal failure - - Familial, X-linked - - - - - Maria João Nabais Sá 00093975
0000072367 53y renal failure; hearing loss; no ocular phenotype; renal failure - - Familial, X-linked - - - - - Maria João Nabais Sá 00093976
0000072368 46y renal failure; hearing loss; no ocular phenotype; renal failure - - Familial, X-linked - - - - - Maria João Nabais Sá 00093977
0000072369 Microscopic hematuria and proteinuria diagnosed at 28 years old; no hearing loss; no renal failure - - Familial, X-linked - - - - - Maria João Nabais Sá 00093978
0000072370 30y renal failure; hearing loss; ocular changes; renal failure - - Familial, X-linked - - - - - Maria João Nabais Sá 00093979
0000072371 32y renal failure; hearing loss; ocular changes; renal failure, lomerulus abnormal - - Familial, X-linked - - - - - Maria João Nabais Sá 00093980
0000072372 64y renal failure; hearing loss; ocular changes; renal failure - - Familial, X-linked - - - - - Maria João Nabais Sá 00093981
0000072373 History of microscopic hematuria and proteinuria; no hearing loss; no ocular phenotype; no renal failure - - Familial, X-linked - - - - - Maria João Nabais Sá 00093982
0000072374 23y renal failure; hearing loss; ocular changes; renal failure, lomerulus abnormal - - Familial, X-linked - - - - - Maria João Nabais Sá 00093983
0000072375 17y renal failure; no hearing loss (subjective); no ocular phenotype; renal failure, lomerulus abnormal - - Familial, X-linked - - - - - Maria João Nabais Sá 00093984
0000072376 16y renal failure; hearing loss; no ocular phenotype; renal failure, lomerulus abnormal - - Familial, X-linked - - - - - Maria João Nabais Sá 00093985
0000072377 18y renal failure; hearing loss; ocular changes; renal failure - - Familial, X-linked - - - - - Maria João Nabais Sá 00093986
0000126689 no hearing loss (-HP:0000365); no ocular changes; GBM pathology scattered electron dense deposits in GBM without diffuse thinning of the GBM; 30y-renal failure (HP:0000083); hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154012
0000126695 no hearing loss (-HP:0000365); no ocular changes; hematuria (HP:0000790); no proteinuria (-HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154018
0000126696 no hearing loss (-HP:0000365); no ocular changes; 25y-renal failure (HP:0000083); hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154019
0000126703 no hearing loss (-HP:0000365); no ocular changes; GBM pathology lamellation; 17y-renal failure (HP:0000083); hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154026
0000126708 hearing loss (HP:0000365); no ocular changes; GBM splitting; hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154031
0000126713 hearing loss (HP:0000365); no ocular changes; GBM pathology lamellation; hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154036
0000126717 GBM pathology lamellation, negative expression for collagen IV a5 chain; hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154040
0000126731 hematuria (HP:0000790); no proteinuria (-HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154054
0000126750 hearing loss (HP:0000365); ocular changes; hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154073
0000126775 hearing loss (HP:0000365); 39y-renal failure (HP:0000083); hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154098
0000126785 diabete; GBM pathology thin basement membrane nephropathy with Focal and segmental glomerulosclerosis; 30y-57yy-renal failure (HP:0000083); hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked 57y - - - - Judy Savige 00154108
0000126787 no hearing loss (-HP:0000365); no ocular changes; GBM pathology Basket-weave changes; hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154110
0000126789 hearing loss (HP:0000365); ocular changes, retinal vessel angiopathy; hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154112
0000126810 no hearing loss (-HP:0000365); no ocular changes; hematuria (HP:0000790); proteinuria (HP:0000093) Alport syndromeymptomatic XL Alport syndrome - Familial, X-linked - - - - - Judy Savige 00154133
0000126814 no hearing loss (-HP:0000365); no ocular changes; GBM pathology thinning, thickening; hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154137
0000126825 hearing loss (HP:0000365); no ocular changes; hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154148
0000126845 no hearing loss (-HP:0000365); no ocular changes; GBM pathology thinned, GBM with dense granules and splitting; hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154168
0000126846 no hearing loss (-HP:0000365); no ocular changes; GBM pathology lamellation; 10y-renal failure (HP:0000083); hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154169
0000126849 hearing loss (HP:0000365); no ocular changes; GBM pathology thinning, thickening, splitting; 20y-renal failure (HP:0000083); hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154172
0000126856 hearing loss (HP:0000365); hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154179
0000126873 hearing loss (HP:0000365); GBM pathology lamellated and ‘basket-weave’ appearance, extensive effacement of podocyte processes; hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154196
0000126876 hearing loss (HP:0000365); ocular changes; hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154199
0000126879 no hearing loss (-HP:0000365); ocular changes; hematuria (HP:0000790); proteinuria (HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154202
0000126928 hematuria (HP:0000790); no proteinuria (-HP:0000093) XL Alport syndrome syndrome, Alport, X-linked recessive (ASXL) Familial, X-linked - - - - - Judy Savige 00154251
0000203420 hematuria, proteinuria hereditary nephritis Alport syndrom Familial, X-linked 08y 08y 06y hematuria - Tamara Nikuseva Martic 00265633
0000270450 - - Alport Syndrome Familial, X-linked - 05y 04y - - Jasmina Comic 00375240
0000270451 - - Alport Syndrome X-linked Familial, X-linked - - - - - Jasmina Comic 00375241
0000270452 - - - Unknown - 72y 08y - - Jasmina Comic 00375242
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