Phthisis bulbi

Symptom Information:

Symptom ID: HPO:0000667
Synonyms:
Phthisis bulbi [OMIM:Phthisis bulbi]
Quality:
Cross references:
OMIM: "Phthisis bulbi" [OMIM:Phthisis bulbi]
Is a (Direct Parents):
HPO         Abnormality of the globe
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Phthisis bulbi(HPO:0000667)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Congenital blindness due to retinal non-attachment (Orphanet:300337)
Knobloch syndrome (Orphanet:1571)
Oculofaciocardiodental syndrome (Orphanet:2712)
Osteoporosis - pseudoglioma (Orphanet:2788)