Entry Search - 140000 142959 - OMIM
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Search: '140000 142959 (Search in: MIM number)'
Results: 2 entries.

1:
* 142959. HOMEOBOX A13; HOXA13
Cytogenetic location: 7p15.2, Genomic coordinates (GRCh38): 7:27,194,364-27,200,091
Matching terms: 142959
► Gene-Phenotype Relationships  ► ICD+  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
7p15.2 ?Guttmacher syndrome 176305 AD 3
Hand-foot-genital syndrome 140000 AD 3
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ICD+
SNOMEDCT: 702425002, 722452004
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2:
# 140000. HAND-FOOT-GENITAL SYNDROME; HFG
Cytogenetic location: 7p15.2
Matching terms: 140000
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
7p15.2 Hand-foot-genital syndrome 140000 AD 3 HOXA13 142959
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ICD+
SNOMEDCT: 702425002
ORPHA: 2438
DO: 0060739
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Search: 140000 142959 (Search in: MIM number)
Results: 2 entries.

1:
* 142959. HOMEOBOX A13; HOXA13
Cytogenetic location: 7p15.2, Genomic coordinates (GRCh38): 7:27,194,364-27,200,091
Matching terms: 142959

2:
# 140000. HAND-FOOT-GENITAL SYNDROME; HFG
Cytogenetic location: 7p15.2
Matching terms: 140000


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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