CUI Disease Vocabulary Name in Vocabulary Code
C1842466 Uniparental disomy, paternal, chromosome 14 MONDO paternal uniparental disomy of chromosome 14 0011975
C1842466 Uniparental disomy, paternal, chromosome 14 MONDO multiple congenital anomalies due to 14q32.2 maternally expressed gene defect 0016779
C1842466 Uniparental disomy, paternal, chromosome 14 MSH Uniparental disomy, paternal, chromosome 14 C536471
C1842466 Uniparental disomy, paternal, chromosome 14 OMIM KAGAMI-OGATA SYNDROME 608149
C1842466 Uniparental disomy, paternal, chromosome 14 OMIM UNIPARENTAL DISOMY, PATERNAL, CHROMOSOME 14 608149
C1842466 Uniparental disomy, paternal, chromosome 14 ORDO Kagami-Ogata syndrome 254519
C1842466 Uniparental disomy, paternal, chromosome 14 ORDO Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14 96334