ID   HPS1913
AC   CVCL_C9Q1
DR   RCB; HPS1913
DR   Wikidata; Q123031949
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C74983; 1p36 deletion syndrome
DI   ORDO; Orphanet_1606; 1p36 deletion syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_C9Q0 ! HPS1912
OI   CVCL_C9Q2 ! HPS1914
OI   CVCL_C9Q3 ! HPS1915
OI   CVCL_C9Q4 ! HPS1916
OI   CVCL_C9Q5 ! HPS1917
SX   Male
AG   10-19Y
CA   Induced pluripotent stem cell
DT   Created: 05-10-23; Last updated: 30-01-24; Version: 2
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