Bone spicule pigmentation of the retina

Symptom Information:

Symptom ID: HPO:0007737
Synonyms:
Bone corpuscle fundus pigmentation [HPO:0007737]
Fundus with peripheral bony spicules [HPO:0007737]
RETINAL 'BONE CORPUSCLE' PIGMENTATION [HPO:0007737]
Retinal bone corpuscle pigmentation [HPO:0007737]
Bone corpuscle fundus pigmentation [OMIM:Bone corpuscle fundus pigmentation]
Bony spicule pigmentary retinopathy [OMIM:Bony spicule pigmentary retinopathy]
Retinal 'bone corpuscle' pigmentation [OMIM:Retinal 'bone corpuscle' pigmentation]
Fundus with peripheral 'bony spicules' [OMIM:Fundus with peripheral 'bony spicules']
Quality:
Cross references:
OMIM: "Bone corpuscle fundus pigmentation" [OMIM:Bone corpuscle fundus pigmentation]
OMIM: "Bony spicule pigmentary retinopathy" [OMIM:Bony spicule pigmentary retinopathy]
OMIM: "Retinal 'bone corpuscle' pigmentation" [OMIM:Retinal 'bone corpuscle' pigmentation]
OMIM: "Fundus with peripheral 'bony spicules'" [OMIM:Fundus with peripheral 'bony spicules']
Is a (Direct Parents):
HPO         Pigmentary retinopathy
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)