Entry Search - 608736 617013 - OMIM
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Search: '608736 617013 (Search in: MIM number)'
Results: 2 entries.

1:
* 608736. SOLUTE CARRIER FAMILY 39 (ZINC TRANSPORTER), MEMBER 14; SLC39A14
Cytogenetic location: 8p21.3, Genomic coordinates (GRCh38): 8:22,367,278-22,434,129
Matching terms: 608736
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
8p21.3 ?Hyperostosis cranalis interna 144755 AD 3
Hypermanganesemia with dystonia 2 617013 AR 3
ICD+
SNOMEDCT: 1217210001, 768554008

2:
# 617013. HYPERMANGANESEMIA WITH DYSTONIA 2; HMNDYT2
Cytogenetic location: 8p21.3
Matching terms: 617013
 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
8p21.3 Hypermanganesemia with dystonia 2 617013 AR 3 SLC39A14 608736
Hypermanganesemia with dystonia - PS613280 - 2 Entries
Location Phenotype Inheritance Phenotype
mapping key
Phenotype
MIM number
Gene/Locus Gene/Locus
MIM number
1q41 Hypermanganesemia with dystonia 1 AR 3 613280 SLC30A10 611146
8p21.3 Hypermanganesemia with dystonia 2 AR 3 617013 SLC39A14 608736
ICD+
SNOMEDCT: 768554008
ORPHA: 521406
DO: 0080537
Search: 608736 617013 (Search in: MIM number)
Results: 2 entries.

1:
* 608736. SOLUTE CARRIER FAMILY 39 (ZINC TRANSPORTER), MEMBER 14; SLC39A14
Cytogenetic location: 8p21.3, Genomic coordinates (GRCh38): 8:22,367,278-22,434,129
Matching terms: 608736

2:
# 617013. HYPERMANGANESEMIA WITH DYSTONIA 2; HMNDYT2
Cytogenetic location: 8p21.3
Matching terms: 617013