Skip to main content
Terminology Service for NFDI4Health
Toggle navigation
Home
Resources
About
Use Cases
Projects
Contact
Terminology Service
Human Phenotype Ontology
HP
HP:0007881
Copy
Central corneal dystrophy
Go to external page
http://purl.obolibrary.org/obo/HP_0007881
Copy
Reset tree
Show siblings
Graph view
Tree view
Term info
Label
Central corneal dystrophy
database cross reference
has obo namespace
human_phenotype
id
HP:0007881
Term relations
Subclass of:
Central opacification of the cornea
