Entry Search - 136680 194070 194080 256370 607102 608978 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '136680 194070 194080 256370 607102 608978 (Search in: MIM number)'
Results: 6 entries.

1:
* 607102. WT1 TRANSCRIPTION FACTOR; WT1
WT1/EWS FUSION GENE, INCLUDED
Cytogenetic location: 11p13, Genomic coordinates (GRCh38): 11:32,387,775-32,435,539
Matching terms: 607102
► Gene-Phenotype Relationships  ► ICD+  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
11p13 Denys-Drash syndrome 194080 AD, SMu 3
Frasier syndrome 136680 AD, SMu 3
Meacham syndrome 608978 AD 3
Mesothelioma, somatic 156240 3
Nephrotic syndrome, type 4 256370 AD 3
Wilms tumor, type 1 194070 AD, SMu 3
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ICD+
SNOMEDCT: 236385009, 25081006, 302849000, 445431000, 722461004
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2:
# 194080. DENYS-DRASH SYNDROME; DDS
Cytogenetic location: 11p13
Matching terms: 194080
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
11p13 Denys-Drash syndrome 194080 AD, SMu 3 WT1 607102
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ICD+
SNOMEDCT: 236385009
ORPHA: 220
DO: 3764
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3:
# 194070. WILMS TUMOR 1; WT1
Cytogenetic locations: 11p13, 13q13.1, Xq26.2
Matching terms: 194070
► Phenotype-Gene Relationships  ► Phenotypic Series  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
11p13 Wilms tumor, type 1 194070 AD, SMu 3 WT1 607102
13q13.1 Wilms tumor 194070 AD, SMu 3 BRCA2 600185
Xq26.2 Wilms tumor, somatic 194070 3 GPC3 300037
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ICD+
SNOMEDCT: 25081006, 302849000
ORPHA: 654
DO: 2154
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4:
# 608978. MEACHAM SYNDROME
Cytogenetic location: 11p13
Matching terms: 608978
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
11p13 Meacham syndrome 608978 AD 3 WT1 607102
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ICD+
SNOMEDCT: 722461004
ORPHA: 3097
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5:
# 136680. FRASIER SYNDROME
Cytogenetic location: 11p13
Matching terms: 136680
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
11p13 Frasier syndrome 136680 AD, SMu 3 WT1 607102
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ICD+
SNOMEDCT: 445431000
ORPHA: 347
DO: 0050438
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6:
# 256370. NEPHROTIC SYNDROME, TYPE 4; NPHS4
Cytogenetic location: 11p13
Matching terms: 256370
► Phenotype-Gene Relationships  ► Phenotypic Series  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
11p13 Nephrotic syndrome, type 4 256370 AD 3 WT1 607102
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Nephrotic syndrome - PS256300 - 26 Entries
Location Phenotype Inheritance Phenotype
mapping key 		Phenotype
MIM number 		Gene/Locus Gene/Locus
MIM number
1q23.1 Nephrotic syndrome, type 23 AR 3 619201 KIRREL1 607428
1q23.3 Nephrotic syndrome, type 22 AR 3 619155 NOS1AP 605551
1q25.2 Nephrotic syndrome, type 2 AR 3 600995 PDCN 604766
1q42.13 Nephrotic syndrome, type 18 AR 3 618177 NUP133 607613
3p21.31 Nephrotic syndrome, type 5, with or without ocular abnormalities AR 3 614199 LAMB2 150325
6p21.2 Nephrotic syndrome, type 24 AR 3 619263 DAAM2 606627
7q21.11 Nephrotic syndrome, type 15 AR 3 617609 MAGI2 606382
7q33 ?Nephrotic syndrome, type 13 AR 3 616893 NUP205 614352
10q22.1 RENI syndrome AR 3 617575 SGPL1 603729
10q23.33 Nephrotic syndrome, type 3 AR 3 610725 PLCE1 608414
11p13 Nephrotic syndrome, type 4 AD 3 256370 WT1 607102
11p11.2 ?Nephrotic syndrome, type 19 AR 3 618178 NUP160 607614
12p12.3 Nephrotic syndrome, type 6 AR 3 614196 PTPRO 600579
12q14.1 Nephrotic syndrome, type 21 AR 3 618594 AVIL 613397
12q15 Nephrotic syndrome, type 11 AR 3 616730 NUP107 607617
16p13.13 Nephrotic syndrome, type 10 AR 3 615861 EMP2 602334
16q13 Nephrotic syndrome, type 12 AR 3 616892 NUP93 614351
17q22 {Hemolytic uremic syndrome, atypical, susceptibility to, 7} AR 3 615008 DGKE 601440
17q22 Nephrotic syndrome, type 7 AR 3 615008 DGKE 601440
17q25.1 Nephrotic syndrome, type 17 AR 3 618176 NUP85 170285
17q25.3 Nephrotic syndrome, type 8 AR 3 615244 ARHGDIA 601925
19p13.2 Nephrotic syndrome, type 16 AR 3 617783 KANK2 614610
19q13.12 Nephrotic syndrome, type 1 AR 3 256300 NPHS1 602716
19q13.2 Nephrotic syndrome, type 9 AR 3 615573 COQ8B 615567
20q13.33 Nephrotic syndrome, type 26 AR 3 620049 LAMA5 601033
Xq22.3 Nephrotic syndrome, type 20 XL 3 301028 TBC1D8B 301027
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ICD+
ORPHA: 656
DO: 0080383
▲ Close
Search: 136680 194070 194080 256370 607102 608978 (Search in: MIM number)
Results: 6 entries.

1:
* 607102. WT1 TRANSCRIPTION FACTOR; WT1
WT1/EWS FUSION GENE, INCLUDED
Cytogenetic location: 11p13, Genomic coordinates (GRCh38): 11:32,387,775-32,435,539
Matching terms: 607102

2:
# 194080. DENYS-DRASH SYNDROME; DDS
Cytogenetic location: 11p13
Matching terms: 194080

3:
# 194070. WILMS TUMOR 1; WT1
Cytogenetic locations: 11p13, 13q13.1, Xq26.2
Matching terms: 194070

4:
# 608978. MEACHAM SYNDROME
Cytogenetic location: 11p13
Matching terms: 608978

5:
# 136680. FRASIER SYNDROME
Cytogenetic location: 11p13
Matching terms: 136680

6:
# 256370. NEPHROTIC SYNDROME, TYPE 4; NPHS4
Cytogenetic location: 11p13
Matching terms: 256370


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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.
Printed: May 30, 2024