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trisomy 12p

Disease Summary
Associated Targets ()

Mondo Description Trisomy 12p is an extremely rare chromosomal disorder (over 30 cases reported worldwide) characterized by craniofacial malformations (round face, prominent cheeks, high bulging forehead, broad and flat nasal bridge, short nose with anteverted nostrils, long philtrum, prominent and everted lower lip, low-set ears, abnormally folded helix, protuberant antihelix), postnatal growth retardation, mental and psychomotor retardation, generalized hypotonia, abnormally short wide hands and/or other abnormalities.
Mondo Term and Equivalent IDs
MONDO:0015723:  trisomy 12p
GARD:0005305: 
MESH:C538299: 
Orphanet:1699: 
UMLS:C0795845: