Ackerman syndrome https://rarediseases.info.nih.gov/diseases/469/ackerman-syndrome https://www.malacards.org/card/ackerman_syndrome pyramidal molars, glaucoma, abnormal upper lip SCTID:722280000 UMLS:C1860167 Ackerman fused molar rooth syndrome juvenile glaucoma with unusual upper lip and dental roots pyramidal molar-glaucoma-upper abnormal lip syndrome OMIM:200970 GARD:0000469 MEDGEN:395426 MONDO:0008706 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. MESH:C538170 Orphanet:2561 icd11.foundation:1946127088 Ackerman syndrome multiple congenital anomalies/dysmorphic syndrome without intellectual disability ectodermal dysplasia syndrome