Congenital primary aphakia

Symptom Information:

Symptom ID: HPO:0007707
Synonyms:
Congenital primary aphakia [OMIM:Congenital primary aphakia]
Quality:
Cross references:
OMIM: "Congenital primary aphakia" [OMIM:Congenital primary aphakia]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the lens
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)
                Aplasia/Hypoplasia affecting the eye(HPO:0008056)
                   Aplasia/Hypoplasia affecting the anterior segment of the eye(HPO:0008062)
                      Aplasia/Hypoplasia of the lens(HPO:0008063)
                         Congenital primary aphakia(HPO:0007707)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Aplasia/Hypoplasia affecting the anterior segment of the eye(HPO:0008062)
                      Aplasia/Hypoplasia of the lens(HPO:0008063)
                         Congenital primary aphakia(HPO:0007707)
                   Abnormality of the lens(HPO:0000517)
                      Aplasia/Hypoplasia of the lens(HPO:0008063)
                         Congenital primary aphakia(HPO:0007707)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Bardet-Biedl syndrome (Orphanet:110)
Congenital primary aphakia (Orphanet:83461)