Entry Search - 276600 613018 - OMIM
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Search: '276600 613018 (Search in: MIM number)'
Results: 2 entries.

1:
* 613018. TYROSINE AMINOTRANSFERASE; TAT
Cytogenetic location: 16q22.2, Genomic coordinates (GRCh38): 16:71,565,660-71,577,092
Matching terms: 613018
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
16q22.2 Tyrosinemia, type II 276600 AR 3
ICD+
SNOMEDCT: 124287008, 4887000

2:
# 276600. TYROSINEMIA, TYPE II; TYRSN2
Cytogenetic location: 16q22.2
Matching terms: 276600
 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
16q22.2 Tyrosinemia, type II 276600 AR 3 TAT 613018
Tyrosinemia - PS276700 - 3 Entries
Location Phenotype Inheritance Phenotype
mapping key
Phenotype
MIM number
Gene/Locus Gene/Locus
MIM number
12q24.31 Tyrosinemia, type III AR 3 276710 HPD 609695
15q25.1 Tyrosinemia, type I AR 3 276700 FAH 613871
16q22.2 Tyrosinemia, type II AR 3 276600 TAT 613018
ICD+
SNOMEDCT: 124287008, 4887000
ORPHA: 28378
DO: 0050725
Search: 276600 613018 (Search in: MIM number)
Results: 2 entries.

1:
* 613018. TYROSINE AMINOTRANSFERASE; TAT
Cytogenetic location: 16q22.2, Genomic coordinates (GRCh38): 16:71,565,660-71,577,092
Matching terms: 613018

2:
# 276600. TYROSINEMIA, TYPE II; TYRSN2
Cytogenetic location: 16q22.2
Matching terms: 276600