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Congenital heart defects, multiple types, 1, X-linked(CHTD1)

MedGen UID:: 463217
•Concept ID:: C3151867
•: Disease or Syndrome

Synonym:	Congenital heart defects, nonsyndromic, 1, X-linked

Monarch Initiative:	MONDO:0800321
OMIM®:	300265; 306955

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Clinical prediction guides

A novel ZIC3 mutation in a Chinese family with heterotaxy and multiple types of congenital heart defect.

Wang Y, Dai X, Liu H, Peng J, Chen J
Prenat Diagn 2023 Mar;43(3):275-279. Epub 2022 Dec 30 doi: 10.1002/pd.6294. PMID: 36567274

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Congenital heart defects, multiple types, 1, X-linked
Congenital heart defects, multiple types, 1, X-linked

MedGen
C3151867[conceptid] (1)
MedGen
C4479246[trait identifier] AND "OMIM"[submitter] (6)
ClinVar
C4539857[trait identifier] AND "OMIM"[submitter] (5)
ClinVar
C4479250[trait identifier] AND "OMIM"[submitter] (2)
ClinVar

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