Entry Search - 611720 618088 - OMIM
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Search: '611720 618088 (Search in: MIM number)'
Results: 2 entries.

1:
* 611720. INTERFERON REGULATORY FACTOR 2-BINDING PROTEIN LIKE; IRF2BPL
Cytogenetic location: 14q24.3, Genomic coordinates (GRCh38): 14:77,024,543-77,028,708
Matching terms: 611720
► Gene-Phenotype Relationships  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
14q24.3 Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures 618088 AD 3
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2:
# 618088. NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS
Cytogenetic location: 14q24.3
Matching terms: 618088
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
14q24.3 Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures 618088 AD 3 IRF2BPL 611720
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ICD+
ORPHA: 597623
DO: 0081327
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Search: 611720 618088 (Search in: MIM number)
Results: 2 entries.

1:
* 611720. INTERFERON REGULATORY FACTOR 2-BINDING PROTEIN LIKE; IRF2BPL
Cytogenetic location: 14q24.3, Genomic coordinates (GRCh38): 14:77,024,543-77,028,708
Matching terms: 611720

2:
# 618088. NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS
Cytogenetic location: 14q24.3
Matching terms: 618088


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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