U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Lichen planus, familial

MedGen UID:
372036
Concept ID:
C1835402
Disease or Syndrome
Synonym: Lichen Planus, Familial
 
Monarch Initiative: MONDO:0007902
OMIM®: 151620

Definition

An instance of lichen planus that is caused by an inherited modification of the individual's genome. [from MONDO]

Clinical features

From HPO
Abnormality of the skin
MedGen UID:
11449
Concept ID:
C0037268
Congenital Abnormality
An abnormality of the skin.

Recent clinical studies

Etiology

Yew YW, Tey HL
Dermatol Ther 2014 Jan-Feb;27(1):12-5. Epub 2013 Mar 25 doi: 10.1111/dth.12023. PMID: 24502303
Jin X, Wang J, Zhu L, Wang L, Dan H, Zeng X, Chen Q
J Dermatol Sci 2012 Dec;68(3):127-34. Epub 2012 Sep 13 doi: 10.1016/j.jdermsci.2012.09.003. PMID: 23021488

Therapy

Yew YW, Tey HL
Dermatol Ther 2014 Jan-Feb;27(1):12-5. Epub 2013 Mar 25 doi: 10.1111/dth.12023. PMID: 24502303

Clinical prediction guides

Yew YW, Tey HL
Dermatol Ther 2014 Jan-Feb;27(1):12-5. Epub 2013 Mar 25 doi: 10.1111/dth.12023. PMID: 24502303

Supplemental Content

Table of contents

    Clinical resources

    Consumer resources

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...