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Linear Hypopigmentation and Craniofacial Asymmetry with Acral, Ocular and Brain Anomalies

Alias:
Rhoa-Related Mosaic Ectodermal Dysplasia
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Linear Hypopigmentation and Craniofacial Asymmetry with Acral, Ocular and Brain Anomalies, is also known as rhoa-related mosaic ectodermal dysplasia. An important gene associated with Linear Hypopigmentation and Craniofacial Asymmetry with Acral, Ocular and Brain Anomalies is RHOA (Ras Homolog Family Member A). Affiliated tissues include skin and brain.
Related ID：
MALACARDS：LNR018

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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No data available Phase
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1
9
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LNR018

Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Related Drugs

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No data available

Disease Model

Category
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MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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