Entry Search - 192315 606609 - OMIM
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Search: '192315 606609 (Search in: MIM number)'
Results: 2 entries.

1:
* 606609. 3-PRIME REPAIR EXONUCLEASE 1; TREX1
Cytogenetic location: 3p21.31, Genomic coordinates (GRCh38): 3:48,465,830-48,467,645
Matching terms: 606609
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
3p21.31 {Systemic lupus erythematosus, susceptibility to} 152700 AD 3
Aicardi-Goutieres syndrome 1, dominant and recessive 225750 AD, AR 3
Chilblain lupus 610448 AD 3
Vasculopathy, retinal, with cerebral leukoencephalopathy and systemic manifestations 192315 AD 3
ICD+
SNOMEDCT: 783787000

2:
# 192315. VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKOENCEPHALOPATHY AND SYSTEMIC MANIFESTATIONS; RVCLS
Cytogenetic location: 3p21.31
Matching terms: 192315
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
3p21.31 Vasculopathy, retinal, with cerebral leukoencephalopathy and systemic manifestations 192315 AD 3 TREX1 606609
ICD+
SNOMEDCT: 783787000
ORPHA: 247691
DO: 0111567
Search: 192315 606609 (Search in: MIM number)
Results: 2 entries.

1:
* 606609. 3-PRIME REPAIR EXONUCLEASE 1; TREX1
Cytogenetic location: 3p21.31, Genomic coordinates (GRCh38): 3:48,465,830-48,467,645
Matching terms: 606609

2:
# 192315. VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKOENCEPHALOPATHY AND SYSTEMIC MANIFESTATIONS; RVCLS
Cytogenetic location: 3p21.31
Matching terms: 192315