Entry Search - 164874 613454 - OMIM
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Search: '164874 613454 (Search in: MIM number)'
Results: 2 entries.

1:
* 164874. FORKHEAD BOX G1; FOXG1
Cytogenetic location: 14q12, Genomic coordinates (GRCh38): 14:28,766,787-28,770,277
Matching terms: 164874
► Gene-Phenotype Relationships  ► ICD+  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
14q12 Rett syndrome, congenital variant 613454 AD 3
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ICD+
SNOMEDCT: 702450004
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2:
# 613454. RETT SYNDROME, CONGENITAL VARIANT
Cytogenetic location: 14q12
Matching terms: 613454
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
14q12 Rett syndrome, congenital variant 613454 AD 3 FOXG1 164874
▲ Close
ICD+
SNOMEDCT: 702450004
ORPHA: 561854
DO: 1206
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Search: 164874 613454 (Search in: MIM number)
Results: 2 entries.

1:
* 164874. FORKHEAD BOX G1; FOXG1
Cytogenetic location: 14q12, Genomic coordinates (GRCh38): 14:28,766,787-28,770,277
Matching terms: 164874

2:
# 613454. RETT SYNDROME, CONGENITAL VARIANT
Cytogenetic location: 14q12
Matching terms: 613454


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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2025 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2025 Johns Hopkins University.
Printed: March 5, 2025