Entry Search - 208050 606145 - OMIM
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Search: '208050 606145 (Search in: MIM number)'
Results: 2 entries.

2:
# 208050. ARTERIAL TORTUOSITY SYNDROME; ATORS
Cytogenetic location: 20q13.12
Matching terms: 208050
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
20q13.12 Arterial tortuosity syndrome 208050 AR 3 SLC2A10 606145
ICD+
SNOMEDCT: 458432002
ICD10CM: Q87.82
ORPHA: 3342
DO: 0050645
Search: 208050 606145 (Search in: MIM number)
Results: 2 entries.

1:
* 606145. SOLUTE CARRIER FAMILY 2 (FACILITATED GLUCOSE TRANSPORTER), MEMBER 10; SLC2A10
Cytogenetic location: 20q13.12, Genomic coordinates (GRCh38): 20:46,708,320-46,736,347
Matching terms: 606145

2:
# 208050. ARTERIAL TORTUOSITY SYNDROME; ATORS
Cytogenetic location: 20q13.12
Matching terms: 208050