Hypoplasia of choroid

Symptom Information:

Symptom ID: HPO:0007757
Synonyms:
Hypoplasia of choroid [OMIM:Hypoplasia of choroid]
Quality:
Cross references:
OMIM: "Hypoplasia of choroid" [OMIM:Hypoplasia of choroid]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the choroid
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)
                Abnormality of the uvea(HPO:0000553)
                   Aplasia/Hypoplasia affecting the uvea(HPO:0008055)
                      Aplasia/Hypoplasia of the choroid(HPO:0001122)
                         Hypoplasia of choroid(HPO:0007757)
                   Abnormality of the choroid(HPO:0000610)
                      Aplasia/Hypoplasia of the choroid(HPO:0001122)
                         Hypoplasia of choroid(HPO:0007757)
                Aplasia/Hypoplasia affecting the eye(HPO:0008056)
                   Aplasia/Hypoplasia affecting the uvea(HPO:0008055)
                      Aplasia/Hypoplasia of the choroid(HPO:0001122)
                         Hypoplasia of choroid(HPO:0007757)
                   Aplasia/Hypoplasia affecting the fundus(HPO:0008057)
                      Aplasia/Hypoplasia of the choroid(HPO:0001122)
                         Hypoplasia of choroid(HPO:0007757)
                Abnormality of the posterior segment of the globe(HPO:0004329)
                   Abnormality of the fundus(HPO:0001098)
                      Abnormality of the choroid(HPO:0000610)
                         Aplasia/Hypoplasia of the choroid(HPO:0001122)
                            Hypoplasia of choroid(HPO:0007757)
                      Aplasia/Hypoplasia affecting the fundus(HPO:0008057)
                         Aplasia/Hypoplasia of the choroid(HPO:0001122)
                            Hypoplasia of choroid(HPO:0007757)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Mulibrey nanism (Orphanet:2576)