Entry Search - 222600 606718 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '222600 606718 (Search in: MIM number)'
Results: 2 entries.

1:
* 606718. SOLUTE CARRIER FAMILY 26 (SULFATE TRANSPORTER), MEMBER 2; SLC26A2
Cytogenetic location: 5q32, Genomic coordinates (GRCh38): 5:149,960,758-149,987,400
Matching terms: 606718
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
5q32 Achondrogenesis Ib 600972 AR 3
Atelosteogenesis, type II 256050 AR 3
De la Chapelle dysplasia 256050 AR 3
Diastrophic dysplasia 222600 AR 3
Diastrophic dysplasia, broad bone-platyspondylic variant 222600 AR 3
Epiphyseal dysplasia, multiple, 4 226900 AR 3
ICD+
SNOMEDCT: 14870002, 254055004, 58561002, 715672007
ICD10CM: Q77.5

2:
# 222600. DIASTROPHIC DYSPLASIA; DTD
DIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED
Cytogenetic locations: 5q32,
Matching terms: 222600
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
5q32 Diastrophic dysplasia 222600 AR 3 SLC26A2 606718
5q32 Diastrophic dysplasia, broad bone-platyspondylic variant 222600 AR 3 SLC26A2 606718
ICD+
SNOMEDCT: 58561002
ICD10CM: Q77.5
ORPHA: 628
DO: 14687
Search: 222600 606718 (Search in: MIM number)
Results: 2 entries.

1:
* 606718. SOLUTE CARRIER FAMILY 26 (SULFATE TRANSPORTER), MEMBER 2; SLC26A2
Cytogenetic location: 5q32, Genomic coordinates (GRCh38): 5:149,960,758-149,987,400
Matching terms: 606718

2:
# 222600. DIASTROPHIC DYSPLASIA; DTD
DIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED
Cytogenetic locations: 5q32,
Matching terms: 222600