Large eyes
Symptom Information:
Symptom ID: | HPO:0001090 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) 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) 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) 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) |