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GHS Goldenhar syndrome [ Homo sapiens (human) ]

Gene ID: 7971, updated on 31-Aug-2024

Summary

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Official Symbol
GHSprovided by HGNC
Official Full Name
Goldenhar syndromeprovided by HGNC
Primary source
MIM:141400
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Bibliography

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Related articles in PubMed

  1. Further evidence for a relationship between the 5p15 chromosome region and the oculoauriculovertebral anomaly. Ala-Mello S, et al. Am J Med Genet A, 2008 Oct 1. PMID 18792983

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Further evidence for a relationship between the 5p15 chromosome region and GHS is reported.
    Title: Further evidence for a relationship between the 5p15 chromosome region and the oculoauriculovertebral anomaly.
Submit: New GeneRIF Correction

Phenotypes

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Associated conditions

Description Tests
Goldenhar syndrome
OMIM: 141400GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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