Buphthalmos

Symptom Information:

Symptom ID: HPO:0000557
Synonyms:
Buphthalmos (finding) [Orphanet:4060]
Hydrophthalmos [Orphanet:4060]
Buphthalmos [OMIM:Buphthalmos]
Buphthalmos [Orphanet:4060]
Developmental glaucoma [Orphanet:4060]
Developmental glaucoma [MedDRA:10012565]
Buphthalmos [MedDRA:10012565]
Buphthalmos associated with other ocular anomalies [MedDRA:10012565]
Buphthalmos, unspecified [MedDRA:10012565]
Buphthalmus [MedDRA:10012565]
Congenital glaucoma [MedDRA:10012565]
Glaucoma congenital [MedDRA:10012565]
Simple buphthalmos [MedDRA:10012565]
Juvenile glaucoma [MedDRA:10012565]
Infantile glaucoma [MedDRA:10012565]
Buphthalmos (WWS) [OMIM:Buphthalmos (WWS)]
Glaucoma, juvenile [OMIM:Glaucoma, juvenile]
Juvenile glaucoma [OMIM:Juvenile glaucoma]
Congenital glaucomas [MedDRA:10018325]
Quality:
Cross references:
Orphanet:4060 "Buphthalmos" [Orphanet:4060]
OMIM: "Buphthalmos" [OMIM:Buphthalmos]
OMIM: "Buphthalmos (WWS)" [OMIM:Buphthalmos (WWS)]
OMIM: "Glaucoma, juvenile" [OMIM:Glaucoma, juvenile]
OMIM: "Juvenile glaucoma" [OMIM:Juvenile glaucoma]
UMLS:C0020302 "Hydrophthalmos" [Orphanet:4060]
Is a (Direct Parents):
Orphanet Abnormality of the eye
MedDRA Glaucoma and ocular hypertension
HPO         Congenital glaucoma
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)
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)