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Disease association ontology term - MONDO:0014507 - Catel-Manzke syndrome

Term summary

ID
MONDO:0014507
Name
Catel-Manzke syndrome
Ontology or CV name
Disease association
Definition
Catel-Manzke syndrome is a rare bone disease characterized by bilateral hyperphalangy and clinodactyly of the index finger typically in association with Pierre Robin sequence comprising micrognathia, cleft palate and glossoptosis.

Parents

Annotation

Disease association

MONDO:0014507 - Catel-Manzke syndrome

References:

Genes: