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odontotrichomelic syndrome

Disease Summary
Associated Targets (0)

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Mondo Description Odontotrichomelic syndrome is characterised 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.
Mondo Term and Equivalent IDs
MONDO:0010111:  odontotrichomelic syndrome
GARD:0002381: 
MESH:C535637: 
Orphanet:2723: 
SCTID:239028001: 
UMLS:CN074199: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found