Global Variome shared LOVD
B3GNT2 (UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosa...)
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Phenotypes for disease #02210 (ATS1 (Alport syndrome, type 1, X-linked), OMIM:301050)
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Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Inheritance
: Indicates the inheritance of the phenotype in the family; unknown, familial (autosomal/X-linked, dominant/ recessive), paternal (Y-linked), maternal (mitochondrial), isolated (sporadic) or complex
All options:
Unknown
Familial
Familial, autosomal dominant
Familial, autosomal recessive
Familial, X-linked
Familial, X-linked dominant
Familial, X-linked dominant, male sparing
Familial, X-linked recessive
Paternal, Y-linked
Maternal, mitochondrial
Isolated (sporadic)
Di-genic
Complex
- = Not applicable
Age/Examination
: age at which the individual was examined.
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Diagnosis
: age diagnosis was confirmed
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Onset
: Age first symptoms disease appeared in individual:
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Phenotype/Onset
: individual's phenotype at Age/Onset described using HPO
Protein
: result from protein staining
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Date
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Date
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Date
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Date
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140 entries on 2 pages. Showing entries 1 - 100.
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Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
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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