Entry Search - 272200 607939 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '272200 607939 (Search in: MIM number)'
Results: 2 entries.

1:
* 607939. SULFATASE-MODIFYING FACTOR 1; SUMF1
Cytogenetic location: 3p26.1, Genomic coordinates (GRCh38): 3:4,034,486-4,467,269
Matching terms: 607939
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
3p26.1 Multiple sulfatase deficiency 272200 AR 3
ICD+
SNOMEDCT: 54898003
ICD10CM: E75.26

2:
# 272200. MULTIPLE SULFATASE DEFICIENCY; MSD
Cytogenetic location: 3p26.1
Matching terms: 272200
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
3p26.1 Multiple sulfatase deficiency 272200 AR 3 SUMF1 607939
ICD+
SNOMEDCT: 54898003
ICD10CM: E75.26
ORPHA: 585
DO: 0050441
Search: 272200 607939 (Search in: MIM number)
Results: 2 entries.

1:
* 607939. SULFATASE-MODIFYING FACTOR 1; SUMF1
Cytogenetic location: 3p26.1, Genomic coordinates (GRCh38): 3:4,034,486-4,467,269
Matching terms: 607939

2:
# 272200. MULTIPLE SULFATASE DEFICIENCY; MSD
Cytogenetic location: 3p26.1
Matching terms: 272200