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Items: 17

  • The following terms were not found in OMIM: 9382, PTA-9382.
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#217095 - CONOTRUNCAL HEART MALFORMATIONS; CTHM

TRUNCUS ARTERIOSUS COMMUNIS, INCLUDED

Cytogenetic locations: 1pter-p36.13, 22q11.21, 1pter-p36.13, 19p13.11, 1pter-p36.13, 18q11.2

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#605472 - USHER SYNDROME, TYPE IIC; USH2C

USHER SYNDROME, TYPE IIC, GPR98/PDZD7, DIGENIC, INCLUDED

Cytogenetic locations: 1pter-p36.13, 5q14.3

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#209920 - BARE LYMPHOCYTE SYNDROME, TYPE II

BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP A, INCLUDED

Cytogenetic locations: 1pter-p36.13, 19p13.11, 1pter-p36.13, 16p13.13

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#300755 - AGAMMAGLOBULINEMIA, X-LINKED; XLA

HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED

Cytogenetic locations: Xq22.1

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