Entry Search - 610661 615273 - OMIM
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Search: '610661 615273 (Search in: MIM number)'
Results: 2 entries.

1:
* 610661. N-GLYCANASE 1; NGLY1
Cytogenetic location: 3p24.2, Genomic coordinates (GRCh38): 3:25,718,944-25,790,039
Matching terms: 610661
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
3p24.2 Congenital disorder of deglycosylation 1 615273 AR 3
ICD+
SNOMEDCT: 768846004

2:
# 615273. CONGENITAL DISORDER OF DEGLYCOSYLATION 1; CDDG1
Cytogenetic location: 3p24.2
Matching terms: 615273
 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
3p24.2 Congenital disorder of deglycosylation 1 615273 AR 3 NGLY1 610661
Congenital disorder of deglycosylation - PS615273 - 2 Entries
Location Phenotype Inheritance Phenotype
mapping key
Phenotype
MIM number
Gene/Locus Gene/Locus
MIM number
3p24.2 Congenital disorder of deglycosylation 1 AR 3 615273 NGLY1 610661
15q24.2 Congenital disorder of deglycosylation 2 AR 3 619775 MAN2C1 154580
ICD+
SNOMEDCT: 768846004
ORPHA: 404454
DO: 0060728
Search: 610661 615273 (Search in: MIM number)
Results: 2 entries.

1:
* 610661. N-GLYCANASE 1; NGLY1
Cytogenetic location: 3p24.2, Genomic coordinates (GRCh38): 3:25,718,944-25,790,039
Matching terms: 610661

2:
# 615273. CONGENITAL DISORDER OF DEGLYCOSYLATION 1; CDDG1
Cytogenetic location: 3p24.2
Matching terms: 615273