Rarefaction of retinal pigmentation
Symptom Information:
| Symptom ID: | HPO:0007961 | ||
| Synonyms: |
|
||
| Quality: | |||
| Cross references: |
|
||
| Is a (Direct Parents): |
|
||
| 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 retina(HPO:0000479) obsolete Abnormality of the retinal pigment epithelium(HPO:0008051) Hypopigmentation of the fundus(HPO:0007894) Rarefaction of retinal pigmentation(HPO:0007961) MedDRA: |
||
| Database Frequency: | 1 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Spondylocarpotarsal synostosis | (Orphanet:3275) |