Entry Search - 268800 606873 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '268800 606873 (Search in: MIM number)'
Results: 2 entries.

1:
* 606873. HEXOSAMINIDASE B; HEXB
ENC1, ANTISENSE, INCLUDED; ENC1AS, INCLUDED
Cytogenetic location: 5q13.3, Genomic coordinates (GRCh38): 5:74,640,023-74,721,288
Matching terms: 606873
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
5q13.3 Sandhoff disease, infantile, juvenile, and adult forms 268800 AR 3
ICD+
SNOMEDCT: 23849003
ICD10CM: E75.01

2:
# 268800. SANDHOFF DISEASE
SANDHOFF DISEASE, ADULT TYPE, INCLUDED
Cytogenetic location: 5q13.3
Matching terms: 268800
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
5q13.3 Sandhoff disease, infantile, juvenile, and adult forms 268800 AR 3 HEXB 606873
ICD+
SNOMEDCT: 23849003
ICD10CM: E75.01
ORPHA: 309155, 309162, 309169, 796
DO: 3323
Search: 268800 606873 (Search in: MIM number)
Results: 2 entries.

1:
* 606873. HEXOSAMINIDASE B; HEXB
ENC1, ANTISENSE, INCLUDED; ENC1AS, INCLUDED
Cytogenetic location: 5q13.3, Genomic coordinates (GRCh38): 5:74,640,023-74,721,288
Matching terms: 606873

2:
# 268800. SANDHOFF DISEASE
SANDHOFF DISEASE, ADULT TYPE, INCLUDED
Cytogenetic location: 5q13.3
Matching terms: 268800