Entry Search - 159555 605130 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '159555 605130 (Search in: MIM number)'
Results: 2 entries.

1:
* 159555. LYSINE-SPECIFIC METHYLTRANSFERASE 2A; KMT2A
MLL/AF4 FUSION GENE, INCLUDED
Cytogenetic location: 11q23.3, Genomic coordinates (GRCh38): 11:118,436,492-118,526,832
Matching terms: 159555
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
11q23.3 Wiedemann-Steiner syndrome 605130 AD 3
ICD+
SNOMEDCT: 763618001

2:
# 605130. WIEDEMANN-STEINER SYNDROME; WDSTS
Cytogenetic location: 11q23.3
Matching terms: 605130
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
11q23.3 Wiedemann-Steiner syndrome 605130 AD 3 KMT2A 159555
ICD+
SNOMEDCT: 763618001
ORPHA: 319182
Search: 159555 605130 (Search in: MIM number)
Results: 2 entries.

1:
* 159555. LYSINE-SPECIFIC METHYLTRANSFERASE 2A; KMT2A
MLL/AF4 FUSION GENE, INCLUDED
Cytogenetic location: 11q23.3, Genomic coordinates (GRCh38): 11:118,436,492-118,526,832
Matching terms: 159555

2:
# 605130. WIEDEMANN-STEINER SYNDROME; WDSTS
Cytogenetic location: 11q23.3
Matching terms: 605130