ID   HPS1551
AC   CVCL_C9UM
DR   RCB; HPS1551
DR   Wikidata; Q123031843
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C75469; Smith-Magenis syndrome
DI   ORDO; Orphanet_819; Smith-Magenis syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_C9UL ! HPS1550
OI   CVCL_C9UN ! HPS1552
OI   CVCL_C9UP ! HPS1553
OI   CVCL_C9UQ ! HPS1554
OI   CVCL_C9UR ! HPS1555
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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