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Xeroderma pigmentosum, type F/Cockayne syndrome(XPF/CS)

MedGen UID:: 812895
•Concept ID:: C3806565
•: Disease or Syndrome

Synonyms:	XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME; XPF/CS

Monarch Initiative:	MONDO:0800313
OMIM®:	133520; 278760

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Xeroderma pigmentosum, type F/Cockayne syndrome
Xeroderma pigmentosum, type F/Cockayne syndrome

MedGen
C3806565[conceptid] (1)
MedGen
C0268141[trait identifier] AND "OMIM"[submitter] (10)
ClinVar
C0268140[trait identifier] AND "OMIM"[submitter] (8)
ClinVar
C1848411[trait identifier] AND "OMIM"[submitter] (4)
ClinVar

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