Increased intraocular pressure
Symptom Information:
Symptom ID: | HPO:0007906 | |||||||||||||||||||||||||||||||||||||||||||||||
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) Increased intraocular pressure(HPO:0007906) Abnormal intraocular pressure(HPO:0012632) Increased intraocular pressure(HPO:0007906) MedDRA: Eye disorders(MedDRA:10015919) Glaucoma and ocular hypertension(MedDRA:10018307) Increased intraocular pressure(HPO:0007906) Glaucoma(HPO:0000501) Increased intraocular pressure(HPO:0007906) Investigations(MedDRA:10022891) Neurological, special senses and psychiatric investigations(MedDRA:10029295) Ophthalmic function diagnostic procedures(MedDRA:10030864) Increased intraocular pressure(HPO:0007906) |
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Database Frequency: | 30 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17q12 microduplication syndrome | (Orphanet:261272) |
Bardet-Biedl syndrome | (Orphanet:110) |
CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES | (OMIM:269400) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Congenital glaucoma | (Orphanet:98976) |
Cutis marmorata telangiectatica congenita | (Orphanet:1556) |
GLAUCOMA 1, OPEN ANGLE, F | (OMIM:603383) |
GLAUCOMA 1, PRIMARY OPEN ANGLE, C | (OMIM:601682) |
GLAUCOMA 3, PRIMARY CONGENITAL, A | (OMIM:231300) |
Glaucoma - ectopia - microspherophakia - stiff joints - short stature | (Orphanet:2084) |
Glaucoma secondary to spherophakia/ectopia lentis and megalocornea | (Orphanet:238763) |
HERNS syndrome | (Orphanet:63261) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Hurler syndrome | (Orphanet:93473) |
IRIS HYPOPLASIA WITH GLAUCOMA | (OMIM:308500) |
Intellectual deficit, X-linked, Armfield type | (Orphanet:85276) |
Mitochondrial myopathy and sideroblastic anemia | (Orphanet:2598) |
Nance-Horan syndrome | (Orphanet:627) |
Oculoauricular syndrome, Schorderet type | (Orphanet:157962) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 5 | (OMIM:613077) |
Proximal renal tubular acidosis | (Orphanet:47159) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
Scheie syndrome | (Orphanet:93474) |
WEILL-MARCHESANI SYNDROME 1 | (OMIM:277600) |
WEILL-MARCHESANI SYNDROME 3 | (OMIM:614819) |
Wolfram syndrome | (Orphanet:3463) |
[DEL] SENGERS SYNDROME | (OMIM:212350) |
[DEL] Wolfram-like syndrome, autosomal dominant | (OMIM:614296) |