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MedGen

National Center for Biotechnology Information

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Items: 3

The following terms were not found in MedGen: 8HH<, Cyrillic.

Select item 1024821.

A rare cutaneous disorder of unknown etiology that can present either as an acute condition, with multiple papular lesions which become vesicular and necrotic (pityriasis lichenoides et varioliformis acuta) or chronic, with small, scaling papules (pityriasis lichenoides chronica). [from NCI]

MedGen UID:: 102482
•Concept ID:: C0162853
•: Disease or Syndrome

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 17921002.

RAC2 Gene Mutation

A change in the nucleotide sequence of the RAC2 gene. [from NCI]

MedGen UID:: 1792100
•Concept ID:: C5555659
•: Cell or Molecular Dysfunction

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 17921013.

Inactivating RAC2 Gene Mutation

A change in the nucleotide sequence of the RAC2 gene that either inhibits expression or results in the translation of an inactive Ras-related C3 botulinum toxin substrate 2 protein. [from NCI]