Aplasia/Hypoplasia of the macula

Symptom Information:

Symptom ID: HPO:0008059
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the retina
HPO         Abnormality of the macula
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)
                Aplasia/Hypoplasia affecting the eye(HPO:0008056)
                   Aplasia/Hypoplasia affecting the fundus(HPO:0008057)
                      Aplasia/Hypoplasia of the retina(HPO:0008061)
                         Aplasia/Hypoplasia of the macula(HPO:0008059)
                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)
                            Aplasia/Hypoplasia of the macula(HPO:0008059)
                         Aplasia/Hypoplasia of the retina(HPO:0008061)
                            Aplasia/Hypoplasia of the macula(HPO:0008059)
                      Aplasia/Hypoplasia affecting the fundus(HPO:0008057)
                         Aplasia/Hypoplasia of the retina(HPO:0008061)
                            Aplasia/Hypoplasia of the macula(HPO:0008059)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

Adult-onset foveomacular vitelliform dystrophy (Orphanet:99000)
Alport syndrome (Orphanet:63)
Aniridia (Orphanet:77)
Best vitelliform macular dystrophy (Orphanet:1243)
Coats disease (Orphanet:190)
EEM syndrome (Orphanet:1897)
Hypotrichosis with juvenile macular degeneration (Orphanet:1573)
Infantile neuronal ceroid lipofuscinosis (Orphanet:79263)
Isolated aniridia (Orphanet:250923)
Knobloch syndrome (Orphanet:1571)
Neuroectodermal melanolysosomal disease (Orphanet:33445)
Ocular albinism (Orphanet:284804)
Oculocutaneous albinism (Orphanet:55)
Oculocutaneous albinism type 1A (Orphanet:79431)
Oculocutaneous albinism type 1B (Orphanet:79434)
Oculocutaneous albinism type 4 (Orphanet:79435)
Sjögren-Larsson syndrome (Orphanet:816)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
Vici syndrome (Orphanet:1493)
Von Hippel-Lindau disease (Orphanet:892)
X-linked recessive ocular albinism (Orphanet:54)