Large eyes

Symptom Information:

Symptom ID: HPO:0001090
Synonyms:
Large eyes [OMIM:Large eyes]
Quality:
Cross references:
OMIM: "Large eyes" [OMIM:Large eyes]
Is a (Direct Parents):
HPO         Abnormality of globe size
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 globe size(HPO:0100887)
                   Large eyes(HPO:0001090)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of globe size(HPO:0100887)
                      Large eyes(HPO:0001090)
                Abnormality of the orbital region(HPO:0000315)
                   Abnormality of globe size(HPO:0100887)
                      Large eyes(HPO:0001090)
MedDRA:
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

3q29 microduplication (Orphanet:251038)
BARTTER SYNDROME, ANTENATAL, TYPE 2 (OMIM:241200)
Bangstad syndrome (Orphanet:1227)
Bartter syndrome (Orphanet:112)
Bird headed-dwarfism, Montreal type (Orphanet:2617)
CRANIOMETADIAPHYSEAL DYSPLASIA (OMIM:269300)
Craniometadiaphyseal dysplasia, wormian bone type (Orphanet:85184)
Frank-Ter Haar syndrome (Orphanet:137834)
Hyperphosphatasia-intellectual deficiency syndrome (Orphanet:247262)
KEPPEN-LUBINSKY SYNDROME (OMIM:614098)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Leprechaunism (Orphanet:508)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 12 (OMIM:615249)
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus (Orphanet:83473)
Micrencephaly - corpus callosum agenesis - abnormal genitalia (Orphanet:2508)
Nakajo-Nishimura syndrome (Orphanet:2615)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Rabson-Mendenhall syndrome (Orphanet:769)
Seckel syndrome (Orphanet:808)
X-linked intellectual deficit, Najm type (Orphanet:163937)