Details of Disease | DrugMAP

General Information of Disease (ID: DIS0INL6)

Disease Name	Atrophoderma vermiculata
Synonyms	folliculitis ulerythematosa reticulata; honeycomb atrophy; Atrophodermia reticulata; atrophoderma vermiculatum; ava; Atrophodermia reticulata symmetrica faciei; Atrophodermia vermiculata; folliculitis ulerythematosa; folliculitis ulerythematosa reticulate; atrophoderma vermiculata
Disease Hierarchy	DISD96XN: Keratosis pilaris atrophicans DIS0INL6: Atrophoderma vermiculata
Disease Identifiers	MONDO ID MONDO_0008849 MESH ID C537412 UMLS CUI C0263429 OMIM ID 209700 MedGen ID 82666 HPO ID HP:0100837 Orphanet ID 79100 SNOMED CT ID 2736005

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 2 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
LRP1	TT9JAGO	Supportive	Autosomal recessive	[1]
LRP1	TTF2V7I	Strong	GermlineCausalMutation	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
LRP1	OTHTEH4G	Supportive	Autosomal recessive	[1]
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References

1	Whole exome sequencing identifies LRP1 as a pathogenic gene in autosomal recessive keratosis pilaris atrophicans. J Med Genet. 2015 Sep;52(9):599-606. doi: 10.1136/jmedgenet-2014-102931. Epub 2015 Jul 3.