Amelogenesis Imperfecta, Type Ih (AI1H)

Alias:
Amelogenesis Imperfecta Type 1h
Ai1h
Amelogenesis Imperfecta, Type 1h
Amelogenesis Imperfecta Type Ih
Amelogenesis Imperfecta 1h
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Amelogenesis Imperfecta, Type Ih, is also known as amelogenesis imperfecta type 1h, and has symptoms including toothache An important gene associated with Amelogenesis Imperfecta, Type Ih is ITGB6 (Integrin Subunit Beta 6). Related phenotypes are anterior open-bite malocclusion and yellow-brown discoloration of the teeth
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
7
5

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
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