Buphthalmos
Symptom Information:
Symptom ID: | HPO:0000557 | |||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the eye(HPO:0000478) Abnormal eye physiology(HPO:0012373) Glaucoma(HPO:0000501) Congenital glaucoma(HPO:0001087) Buphthalmos(HPO:0000557) MedDRA: Eye disorders(MedDRA:10015919) Glaucoma and ocular hypertension(MedDRA:10018307) Buphthalmos(HPO:0000557) |
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Database Frequency: | 16 / 7739 | |||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Ackerman syndrome | (Orphanet:2561) |
CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES | (OMIM:269400) |
Congenital blindness due to retinal non-attachment | (Orphanet:300337) |
Congenital glaucoma | (Orphanet:98976) |
FECHTNER SYNDROME | (OMIM:153640) |
Frank-Ter Haar syndrome | (Orphanet:137834) |
GLAUCOMA 3, PRIMARY CONGENITAL, A | (OMIM:231300) |
IRIDOGONIODYSGENESIS, TYPE 1 | (OMIM:601631) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 | (OMIM:236670) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 | (OMIM:613150) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 | (OMIM:253280) |
Muscle-eye-brain disease | (Orphanet:588) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Proteus syndrome | (Orphanet:744) |
Saethre-Chotzen syndrome | (Orphanet:794) |
Sturge-Weber syndrome | (Orphanet:3205) |