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AIH3 amelogenesis imperfecta 3, hypomaturation or hypoplastic type [ Homo sapiens (human) ]

Gene ID: 201, updated on 31-Aug-2024

Summary

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Official Symbol
AIH3provided by HGNC
Official Full Name
amelogenesis imperfecta 3, hypomaturation or hypoplastic typeprovided by HGNC
Primary source
MIM:301201
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

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Location:
Xq22-q28

Bibliography

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Related articles in PubMed

  1. Genetic heterogeneity in X-linked amelogenesis imperfecta. Aldred MJ, et al. Genomics, 1992 Nov. PMID 1358807

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
amelogenesis imperfecta 3, hypomaturation or hypoplastic type
OMIM: 301201GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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