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Ornithinemia

Alias:
Hyperornithinemia
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Ornithinemia, also known as hyperornithinemia, is related to gyrate atrophy of choroid and retina and night blindness, congenital stationary, autosomal dominant 2. An important gene associated with Ornithinemia is OAT (Ornithine Aminotransferase). Affiliated tissues include retina and brain.
Related ID：
MALACARDS：ORN004

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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1
5
11
ORN004

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

Name
CAS Number
Status
Phase
No data available

Disease Model

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

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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