Abnormality of the choroid

Symptom Information:

Symptom ID: HPO:0000610
Synonyms:
Choroid disease [HPO:0000610]
Choroidal anomaly [Orphanet:4780]
Congenital anomaly of choroid (disorder) [Orphanet:4780]
Congenital anomaly of choroid [Orphanet:4780]
Choroidal anomalies/atrophy/choroideremia [Orphanet:4780]
Congenital choroidal anomaly [Orphanet:4780]
Congenital choroidal anomaly [MedDRA:10057886]
Quality:
Cross references:
Orphanet:4780 "Choroidal anomalies/atrophy/choroideremia" [Orphanet:4780]
UMLS:C0521563 "Congenital anomaly of choroid" [Orphanet:4780]
Is a (Direct Parents):
Orphanet Abnormality of the eye
HPO         Abnormality of the uvea
HPO         Abnormality of the fundus
MedDRA Iris and choroid disorders congenital
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 posterior segment of the globe(HPO:0004329)
                   Abnormality of the fundus(HPO:0001098)
                      Abnormality of the choroid(HPO:0000610)
                Abnormality of the uvea(HPO:0000553)
                   Abnormality of the choroid(HPO:0000610)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Eye disorders congenital(MedDRA:10015920)
       Iris and choroid disorders congenital(MedDRA:10022946)
          Abnormality of the choroid(HPO:0000610)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Adult-onset foveomacular vitelliform dystrophy (Orphanet:99000)
Best vitelliform macular dystrophy (Orphanet:1243)
Blau syndrome (Orphanet:90340)
CHOROIDAL OSTEOMA, BILATERAL (OMIM:118865)
Classic Bartter syndrome (Orphanet:93605)
Focal dermal hypoplasia (Orphanet:2092)
Nanophthalmia (Orphanet:35612)
Oculocerebrofacial syndrome, Kaufman type (Orphanet:2707)
Sinus node disease and myopia (OMIM:182190)
Sturge-Weber syndrome (Orphanet:3205)
Van den Bosch syndrome (Orphanet:3417)