Disease association ontology term - MONDO:0024552 - linear skin defects with multiple congenital anomalies 1
Term summary
- ID
- MONDO:0024552
- Name
- linear skin defects with multiple congenital anomalies 1
- Ontology or CV name
- Disease association
- Definition
- Any microphthalmia with linear skin defects syndrome in which the cause of the disease is a mutation in the HCCS gene.
