Cherry red spot of the macula

Symptom Information:

Symptom ID: HPO:0010729
Synonyms:
Macular cherry-red spot anomaly [Orphanet:5180]
Cherry red spot [HPO:0010729]
Cherry red spot (finding) [Orphanet:5180]
Cherry red spot [Orphanet:5180]
Macular pigmentary anomaly/cherry-red spot [Orphanet:5180]
Cherry red spots [OMIM:Cherry red spots]
Cherry-red spot (type II, infantile and juvenile and type I) [OMIM:Cherry-red spot (type II, infantile and juvenile and type I)]
Quality:
Cross references:
Orphanet:5180 "Macular pigmentary anomaly/cherry-red spot" [Orphanet:5180]
OMIM: "Cherry red spots" [OMIM:Cherry red spots]
OMIM: "Cherry-red spot (type II, infantile and juvenile and type I)" [OMIM:Cherry-red spot (type II, infantile and juvenile and type I)]
UMLS:C0278234 "Cherry red spot" [Orphanet:5180]
Is a (Direct Parents):
Orphanet Abnormality of macular pigmentation
HPO         Abnormality of the macula
Orphanet Abnormality of the eye
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)
                         Abnormality of the macula(HPO:0001103)
                            Cherry red spot of the macula(HPO:0010729)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Farber lipogranulomatosis (Orphanet:333)
GM1 gangliosidosis (Orphanet:354)
Galactosialidosis (Orphanet:351)
Niemann-Pick disease type A (Orphanet:77292)
Sandhoff disease (Orphanet:796)
Sandhoff disease, adult form (Orphanet:309169)
Sandhoff disease, infantile form (Orphanet:309155)
Sandhoff disease, juvenile form (Orphanet:309162)
Sialidosis type 1 (Orphanet:812)
Tay-Sachs disease (Orphanet:845)