Preferred Label : Petty Laxova Wiedemann syndrome;
UMLS semantic type : T047 - Disease or Syndrome;
Origin ID : M0532347;
UMLS CUI : C2931653;
Currated CISMeF NLP mapping
Semantic type(s)
UMLS correspondences (same concept)
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=2963
2014
false
true
false
France
scientific and technical information
progeroid syndrome, congenital, petty type
syndrome
Petty Laxova Wiedemann syndrome
progeroid syndrome, congenital, petty type
---