odontotrichomelic syndrome
MONDO:0010111Mondo
Findings
No curated finding names odontotrichomelic syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Odontotrichomelic syndrome is characterized by malformations of all four extremities, hypoplastic nails, ear anomalies, hypotrichosis, abnormal dentition, hyperhidrosis and nasolacrimal duct obstruction. So far, it has been described in less than 10 patients. Transmission is autosomal recessive.
Definition from the Mondo Disease Ontology (MONDO:0010111), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
4 names
Resolves to: odontotrichomelic syndrome
- Also called
- Freire-Maia odontotrichomelic syndromeFreire-Maia syndromeodontotrichomelic hypohidrotic dysplasiatetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities