Entry Search - 605515 613670 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '605515 613670 (Search in: MIM number)'
Results: 2 entries.

1:
* 605515. FORKHEAD BOX P1; FOXP1
Cytogenetic location: 3p13, Genomic coordinates (GRCh38): 3:70,954,708-71,583,978
Matching terms: 605515
 Gene-Phenotype Relationships   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
3p13 Intellectual developmental disorder with language impairment with or without autistic features 613670 AD 3

2:
# 613670. INTELLECTUAL DEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES; IDDLA
Cytogenetic location: 3p13
Matching terms: 613670
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
3p13 Intellectual developmental disorder with language impairment with or without autistic features 613670 AD 3 FOXP1 605515
ICD+
ORPHA: 391372
DO: 0111331
Search: 605515 613670 (Search in: MIM number)
Results: 2 entries.

1:
* 605515. FORKHEAD BOX P1; FOXP1
Cytogenetic location: 3p13, Genomic coordinates (GRCh38): 3:70,954,708-71,583,978
Matching terms: 605515

2:
# 613670. INTELLECTUAL DEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES; IDDLA
Cytogenetic location: 3p13
Matching terms: 613670