Abnormality of retinal pigmentation

Symptom Information:

Symptom ID: HPO:0007703
Synonyms:
Abnormal retinal pigmentation [OMIM:Abnormal retinal pigmentation]
Quality:
Cross references:
OMIM: "Abnormal retinal pigmentation" [OMIM:Abnormal retinal pigmentation]
Is a (Direct Parents):
HPO         obsolete Abnormality of the retinal pigment epithelium
HPO         Nummular pigmentation of the retina
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)
                            Abnormality of retinal pigmentation(HPO:0007703)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 4 (Orphanet:67048)
Alström syndrome (Orphanet:64)
Alström syndrome (Orphanet:64)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Autosomal recessive chorioretinopathy-microcephaly (Orphanet:2518)
Bardet-Biedl syndrome (Orphanet:110)
Bietti crystalline dystrophy (Orphanet:41751)
CONE-ROD DYSTROPHY 8 (OMIM:605549)
GROUPED PIGMENTATION OF THE RETINA (OMIM:233800)
HYPERREFLEXIA (OMIM:145290)
HYPERREFLEXIA (OMIM:145290)
Homocarnosinosis (Orphanet:2168)
Hurler-Scheie syndrome (Orphanet:93476)
Kearns-Sayre syndrome (Orphanet:480)
MELAS (Orphanet:550)
Mucopolysaccharidosis type 2 (Orphanet:580)
NARP syndrome (Orphanet:644)
Primary hyperoxaluria type 1 (Orphanet:93598)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
Werner syndrome (Orphanet:902)
X-linked cone dysfunction syndrome with myopia (Orphanet:90001)