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Cellosaurus DSH3PV (CVCL_L869)

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Cell line name DSH3PV
Synonyms Dyschromatosis Symmetrica Hereditaria 3 PaVia
Accession CVCL_L869
Resource Identification Initiative To cite this cell line use: DSH3PV (RRID:CVCL_L869)
Comments From: Istituto di Genetica Biochimica ed Evoluzionistica (IGBE); Pavia; Italy.
Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Dyschromatosis symmetrica hereditaria (NCIt: C118435)
Dyschromatosis symmetrica hereditaria (ORDO: Orphanet_41)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 14Y
Category Finite cell line
Cross-references
Cell line databases/resources CLO; CLO_0002832
CLDB; cl1104
Encyclopedic resources Wikidata; Q54831453
Entry history
Entry creation06-May-2013
Last entry update29-Jun-2023
Version number9