Entry Search - 236730 608869 613469 615112 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '236730 608869 613469 615112 (Search in: MIM number)'
Results: 4 entries.

1:
# 615112. UROFACIAL SYNDROME 2; UFS2
Cytogenetic location: 1p13.2
Matching terms: 615112
► 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
1p13.2 Urofacial syndrome 2 615112 AR 3 LRIG2 608869
▲ Close
Urofacial syndrome - PS236730 - 2 Entries
Location Phenotype Inheritance Phenotype
mapping key 		Phenotype
MIM number 		Gene/Locus Gene/Locus
MIM number
1p13.2 Urofacial syndrome 2 AR 3 615112 LRIG2 608869
10q24.2 Urofacial syndrome 1 AR 3 236730 HPSE2 613469
▲ Close
ICD+
ORPHA: 2704
DO: 0050816
▲ Close

2:
# 236730. UROFACIAL SYNDROME 1; UFS1
Cytogenetic location: 10q24.2
Matching terms: 236730
► 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
10q24.2 Urofacial syndrome 1 236730 AR 3 HPSE2 613469
▲ Close
Urofacial syndrome - PS236730 - 2 Entries
Location Phenotype Inheritance Phenotype
mapping key 		Phenotype
MIM number 		Gene/Locus Gene/Locus
MIM number
1p13.2 Urofacial syndrome 2 AR 3 615112 LRIG2 608869
10q24.2 Urofacial syndrome 1 AR 3 236730 HPSE2 613469
▲ Close
ICD+
SNOMEDCT: 236533008
ORPHA: 2704
DO: 0050816
▲ Close

3:
* 608869. LEUCINE-RICH REPEATS- AND IMMUNOGLOBULIN-LIKE DOMAINS-CONTAINING PROTEIN 2; LRIG2
Cytogenetic location: 1p13.2, Genomic coordinates (GRCh38): 1:113,073,198-113,132,260
Matching terms: 608869
► Gene-Phenotype Relationships  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
1p13.2 Urofacial syndrome 2 615112 AR 3
▲ Close

4:
* 613469. HEPARANASE 2; HPSE2
Cytogenetic location: 10q24.2, Genomic coordinates (GRCh38): 10:98,457,077-99,315,951
Matching terms: 613469
► Gene-Phenotype Relationships  ► ICD+  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
10q24.2 Urofacial syndrome 1 236730 AR 3
▲ Close
ICD+
SNOMEDCT: 236533008
▲ Close
Search: 236730 608869 613469 615112 (Search in: MIM number)
Results: 4 entries.

1:
# 615112. UROFACIAL SYNDROME 2; UFS2
Cytogenetic location: 1p13.2
Matching terms: 615112

2:
# 236730. UROFACIAL SYNDROME 1; UFS1
Cytogenetic location: 10q24.2
Matching terms: 236730

3:
* 608869. LEUCINE-RICH REPEATS- AND IMMUNOGLOBULIN-LIKE DOMAINS-CONTAINING PROTEIN 2; LRIG2
Cytogenetic location: 1p13.2, Genomic coordinates (GRCh38): 1:113,073,198-113,132,260
Matching terms: 608869

4:
* 613469. HEPARANASE 2; HPSE2
Cytogenetic location: 10q24.2, Genomic coordinates (GRCh38): 10:98,457,077-99,315,951
Matching terms: 613469


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® 1966-2025 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® 1966-2025 Johns Hopkins University.
Printed: March 5, 2025