Hypoplasia of the retina

Symptom Information:

Symptom ID: HPO:0007770
Synonyms:
Retinal hypoplasia [OMIM:Retinal hypoplasia]
Quality:
Cross references:
OMIM: "Retinal hypoplasia" [OMIM:Retinal hypoplasia]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia 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)
                      Aplasia/Hypoplasia affecting the fundus(HPO:0008057)
                         Aplasia/Hypoplasia of the retina(HPO:0008061)
                            Hypoplasia of the retina(HPO:0007770)
                      Abnormality of the retina(HPO:0000479)
                         Aplasia/Hypoplasia of the retina(HPO:0008061)
                            Hypoplasia of the retina(HPO:0007770)
                Aplasia/Hypoplasia affecting the eye(HPO:0008056)
                   Aplasia/Hypoplasia affecting the fundus(HPO:0008057)
                      Aplasia/Hypoplasia of the retina(HPO:0008061)
                         Hypoplasia of the retina(HPO:0007770)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Histiocytoid cardiomyopathy (Orphanet:137675)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 (OMIM:253280)
POLYCYSTIC KIDNEY, CATARACT, AND CONGENITAL BLINDNESS (OMIM:263100)