Bone spicule pigmentation of the retina
Symptom Information:
Symptom ID: | HPO:0007737 | ||||||||
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) Pigmentary retinopathy(HPO:0000580) Bone spicule pigmentation of the retina(HPO:0007737) MedDRA: |
||||||||
Database Frequency: | 26 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Bardet-Biedl syndrome 1 | (OMIM:209900 ) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bardet-Biedl syndrome 5 | (OMIM:615983) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
Microphthalmia - retinitis pigmentosa - foveoschisis - optic disc drusen | (Orphanet:251279) |
NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1 | (OMIM:610445) |
Pigmented paravenous retinochoroidal atrophy | (Orphanet:251295) |
Posterior column ataxia - retinitis pigmentosa | (Orphanet:88628) |
RETINITIS PIGMENTOSA 1 | (OMIM:180100) |
RETINITIS PIGMENTOSA 19 | (OMIM:601718) |
RETINITIS PIGMENTOSA 25 | (OMIM:602772) |
RETINITIS PIGMENTOSA 28 | (OMIM:606068) |
RETINITIS PIGMENTOSA 30 | (OMIM:607921) |
RETINITIS PIGMENTOSA 33 | (OMIM:610359) |
RETINITIS PIGMENTOSA 36 | (OMIM:610599) |
RETINITIS PIGMENTOSA 39 | (OMIM:613809) |
RETINITIS PIGMENTOSA 45 | (OMIM:613767) |
RETINITIS PIGMENTOSA 51 | (OMIM:613464) |
RETINITIS PIGMENTOSA 54 | (OMIM:613428) |
RETINITIS PIGMENTOSA 58 | (OMIM:613617) |
RETINITIS PIGMENTOSA 61 | (OMIM:614180) |
RETINITIS PIGMENTOSA 9 | (OMIM:180104) |
RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT | (OMIM:180210) |
Retinitis pigmentosa | (Orphanet:791) |
Retinitis pigmentosa 10 | (OMIM:180105) |