Entry Search - 607407 617330 - OMIM
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Search: '607407 617330 (Search in: MIM number)'
Results: 2 entries.

1:
* 607407. EARLY B-CELL FACTOR 3; EBF3
ENHANCER hs737, INCLUDED
Cytogenetic location: 10q26.3, Genomic coordinates (GRCh38): 10:129,835,233-129,964,274
Matching terms: 607407
► Gene-Phenotype Relationships  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
10q26.3 Hypotonia, ataxia, and delayed development syndrome 617330 AD 3
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2:
# 617330. HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS
Cytogenetic location: 10q26.3
Matching terms: 617330
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
10q26.3 Hypotonia, ataxia, and delayed development syndrome 617330 AD 3 EBF3 607407
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ICD+
ORPHA: 658843
DO: 0081176
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Search: 607407 617330 (Search in: MIM number)
Results: 2 entries.

1:
* 607407. EARLY B-CELL FACTOR 3; EBF3
ENHANCER hs737, INCLUDED
Cytogenetic location: 10q26.3, Genomic coordinates (GRCh38): 10:129,835,233-129,964,274
Matching terms: 607407

2:
# 617330. HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS
Cytogenetic location: 10q26.3
Matching terms: 617330


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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 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® 1966-2024 Johns Hopkins University.
Printed: April 28, 2024