Hypopigmentation of the fundus

Symptom Information:

Symptom ID: HPO:0007894
Synonyms:
Decreased retinal pigmentation [HPO:0007894]
Retinal depigmentation [HPO:0007894]
Retinal hypopigmentation [HPO:0007894]
Decreased retinal pigmentation [OMIM:Decreased retinal pigmentation]
Hypopigmentation of the fundus [OMIM:Hypopigmentation of the fundus]
Retinal depigmentation [OMIM:Retinal depigmentation]
Retinal hypopigmentation [OMIM:Retinal hypopigmentation]
Retinal depigmentation [MedDRA:10038846]
Quality:
Cross references:
OMIM: "Decreased retinal pigmentation" [OMIM:Decreased retinal pigmentation]
OMIM: "Hypopigmentation of the fundus" [OMIM:Hypopigmentation of the fundus]
OMIM: "Retinal depigmentation" [OMIM:Retinal depigmentation]
OMIM: "Retinal hypopigmentation" [OMIM:Retinal hypopigmentation]
Is a (Direct Parents):
HPO         obsolete Abnormality of the retinal pigment epithelium
MedDRA Retinal structural change, deposit and degeneration
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)
MedDRA:
Eye disorders(MedDRA:10015919)
    Ocular structural change, deposit and degeneration NEC(MedDRA:10042261)
       Retinal structural change, deposit and degeneration(MedDRA:10038896)
          Hypopigmentation of the fundus(HPO:0007894)
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

ABCD SYNDROME (OMIM:600501)
Acrocallosal syndrome (Orphanet:36)
DILUTION, PIGMENTARY (OMIM:126070)
Familial vascular leukoencephalopathy (Orphanet:36383)
Hermansky-Pudlak syndrome type 9 (Orphanet:280663)
Hyperornithinemia-hyperammonemia-homocitrullinuria (Orphanet:415)
Oculocutaneous albinism type 2 (Orphanet:79432)
Oculocutaneous albinism type 4 (Orphanet:79435)
RETINITIS PIGMENTOSA 13 (OMIM:600059)
Temperature-sensitive oculocutaneous albinism type 1 (Orphanet:352737)
Tietz syndrome (Orphanet:42665)
Vici syndrome (Orphanet:1493)
WAARDENBURG SYNDROME, TYPE 2E (OMIM:611584)
Waardenburg syndrome type 1 (Orphanet:894)