Entry Search - 500008 561000 580000 590080 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '500008 561000 580000 590080 (Search in: MIM number)'
Results: 4 entries.

4:
# 580000. DEAFNESS, AMINOGLYCOSIDE-INDUCED
Cytogenetic location: 22q13.31
Matching terms: 580000
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
22q13.31 {Deafness, mitochondrial, modifier of} 580000 Mi 3 TRMU 610230
ICD+
ORPHA: 90641
DO: 0111734
Search: 500008 561000 580000 590080 (Search in: MIM number)
Results: 4 entries.

1:
* 590080. TRANSFER RNA, MITOCHONDRIAL, SERINE, 1; MTTS1
Matching terms: 590080

2:
* 561000. RIBOSOMAL RNA, MITOCHONDRIAL, 12S; MTRNR1
Matching terms: 561000

3:
# 500008. DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL
Matching terms: 500008

4:
# 580000. DEAFNESS, AMINOGLYCOSIDE-INDUCED
Cytogenetic location: 22q13.31
Matching terms: 580000