Congenital glaucoma
Symptom Information:
| Symptom ID: | HPO:0001087 | ||||
| Synonyms: |
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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) MedDRA: Eye disorders(MedDRA:10015919) Glaucoma and ocular hypertension(MedDRA:10018307) Congenital glaucoma(HPO:0001087) |
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| Database Frequency: | 12 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Aniridia - renal agenesis - psychomotor retardation | (Orphanet:1064) |
| BOWEN SYNDROME OF MULTIPLE MALFORMATIONS | (OMIM:211200) |
| DESBUQUOIS DYSPLASIA 1 | (OMIM:251450) |
| Desbuquois syndrome | (Orphanet:1425) |
| FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA | (OMIM:229310) |
| Histiocytoid cardiomyopathy | (Orphanet:137675) |
| Larsen-like syndrome, B3GAT3 type | (Orphanet:284139) |
| Neonatal diabetes - congenital hypothyroidism - congenital glaucoma - hepatic fibrosis - polycystic kidneys | (Orphanet:79118) |
| PYCR1-related DeBarsy syndrome | (Orphanet:293633) |
| Permanent neonatal diabetes mellitus | (Orphanet:99885) |
| Peters anomaly | (Orphanet:708) |
| TETRALOGY OF FALLOT AND GLAUCOMA | (OMIM:187501) |