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Ackerman syndrome

Disease Summary
Associated Targets (0)

Explore Associated Targets
Mondo Description Ackerman syndrome is characterized by pyramidal molar roots and taurodontism, associated with variable anomalies. It has been described in two generations of one family. Both parents and their six sibs had pyramidal, taurodont or fused molar roots. Some of the patients also had hypotrichosis, an abnormal upper lip, thickened and wide philtrum, and/or juvenile glaucoma. Other features included entropion of the eyelid, syndactyly and clinodactyly of the fifth fingers.
Mondo Term and Equivalent IDs
MONDO:0008706:  Ackerman syndrome
GARD:0000469: 
MESH:C538170: 
Orphanet:2561: 
SCTID:722280000: 
UMLS:C1860167: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found