Ackerman syndrome
MONDO:0008706Mondo
Findings
No curated finding names Ackerman syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0008706), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
2 names
Resolves to: Ackerman syndrome
- Also called
- Ackerman fused molar rooth syndromepyramidal molar-glaucoma-upper abnormal lip syndrome