Dyschromatosis Universalis Hereditaria 3 (DUH3)

Alias:
Duh3
Dyschromatosis Universalis Hereditaria, Type 3
Symmetric Dyschromatosis of the Extremities
Symmetrical Dyschromatosis of Extremities
Dyschromatosis Symmetrica Hereditaria
Reticulate Acropigmentation of Dohi
Dsh
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Dyschromatosis Universalis Hereditaria 3, also known as duh3, is related to dyschromatosis symmetrica hereditaria and dyschromatosis universalis hereditaria 1. An important gene associated with Dyschromatosis Universalis Hereditaria 3 is ABCB6 (ATP Binding Cassette Subfamily B Member 6 (Langereis Blood Group)). Affiliated tissues include skin and spinal cord, and related phenotypes are hypermelanotic macule and hypopigmented macule
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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1
5
2

Medical Symptom

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Gene & Mutation

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Disease Model

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Publications
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References Literature

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