Entry Search - 611055 619000 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '611055 619000 (Search in: MIM number)'
Results: 2 entries.

1:
* 611055. SET DOMAIN-CONTAINING PROTEIN 1B; SETD1B
Cytogenetic location: 12q24.31, Genomic coordinates (GRCh38): 12:121,790,155-121,832,656
Matching terms: 611055
 Gene-Phenotype Relationships   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
12q24.31 Intellectual developmental disorder with seizures and language delay 619000 AD 3

2:
# 619000. INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEIZURES AND LANGUAGE DELAY; IDDSELD
Cytogenetic location: 12q24.31
Matching terms: 619000
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
12q24.31 Intellectual developmental disorder with seizures and language delay 619000 AD 3 SETD1B 611055
ICD+
ORPHA: 528084
Search: 611055 619000 (Search in: MIM number)
Results: 2 entries.

1:
* 611055. SET DOMAIN-CONTAINING PROTEIN 1B; SETD1B
Cytogenetic location: 12q24.31, Genomic coordinates (GRCh38): 12:121,790,155-121,832,656
Matching terms: 611055

2:
# 619000. INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEIZURES AND LANGUAGE DELAY; IDDSELD
Cytogenetic location: 12q24.31
Matching terms: 619000