Hypoplasia of the fovea

Symptom Information:

Symptom ID: HPO:0007750
Synonyms:
Foveal hypoplasia [HPO:0007750]
Foveal hypoplasia [OMIM:Foveal hypoplasia]
Quality:
Cross references:
OMIM: "Foveal hypoplasia" [OMIM:Foveal hypoplasia]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the fovea
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)
                            Aplasia/Hypoplasia of the macula(HPO:0008059)
                               Aplasia/Hypoplasia of the fovea(HPO:0008060)
                                  Hypoplasia of the fovea(HPO:0007750)
                      Abnormality of the retina(HPO:0000479)
                         Abnormality of the macula(HPO:0001103)
                            Abnormality of the fovea(HPO:0000493)
                               Aplasia/Hypoplasia of the fovea(HPO:0008060)
                                  Hypoplasia of the fovea(HPO:0007750)
                            Aplasia/Hypoplasia of the macula(HPO:0008059)
                               Aplasia/Hypoplasia of the fovea(HPO:0008060)
                                  Hypoplasia of the fovea(HPO:0007750)
                         Aplasia/Hypoplasia of the retina(HPO:0008061)
                            Aplasia/Hypoplasia of the macula(HPO:0008059)
                               Aplasia/Hypoplasia of the fovea(HPO:0008060)
                                  Hypoplasia of the fovea(HPO:0007750)
                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)
                            Aplasia/Hypoplasia of the fovea(HPO:0008060)
                               Hypoplasia of the fovea(HPO:0007750)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

FOVEAL HYPOPLASIA 2 (OMIM:609218)
Foveal hypoplasia - presenile cataract (Orphanet:2253)
Isolated aniridia (Orphanet:250923)
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6 (OMIM:613703)
Minimal pigment oculocutaneous albinism type 1 (Orphanet:352734)
Ocular albinism with congenital sensorineural deafness (Orphanet:352740)
Oculocutaneous albinism type 1 (Orphanet:352731)
Oculocutaneous albinism type 1A (Orphanet:79431)
Oculocutaneous albinism type 2 (Orphanet:79432)
Oculocutaneous albinism type 5 (Orphanet:370091)
Åland Islands eye disease (Orphanet:178333)