Glaucoma

Symptom Information:

Symptom ID: HPO:0000501
Synonyms:
Raised intraocular pressure (finding) [Orphanet:4040]
Glaucoma (disorder) [Orphanet:4040]
Glaucoma [Orphanet:4040]
Raised intraocular pressure [Orphanet:4040]
Glaucoma [OMIM:Glaucoma]
Glaucoma [MedDRA:10018304]
Corticosteroid-induced glaucoma [MedDRA:10018304]
Corticosteroid-induced glaucoma, glaucomatous stage [MedDRA:10018304]
Corticosteroid-induced glaucoma, residual stage [MedDRA:10018304]
Glaucoma (excl congenital) [MedDRA:10018304]
Glaucoma associated with anomalies of iris [MedDRA:10018304]
Glaucoma associated with congenital anomalies, dystrophies, and systemic syndromes [MedDRA:10018304]
Glaucoma associated with disorders of the lens [MedDRA:10018304]
Glaucoma associated with ocular inflammations [MedDRA:10018304]
Glaucoma associated with other anterior segment anomalies [MedDRA:10018304]
Glaucoma associated with other lens disorders [MedDRA:10018304]
Glaucoma associated with other ocular disorders [MedDRA:10018304]
Glaucoma associated with systemic syndromes [MedDRA:10018304]
Glaucoma associated with tumors or cysts [MedDRA:10018304]
Glaucoma associated with unspecified ocular disorder [MedDRA:10018304]
Glaucoma associated with vascular disorders [MedDRA:10018304]
Glaucoma both eyes [MedDRA:10018304]
Glaucoma NOS [MedDRA:10018304]
Glaucoma of childhood [MedDRA:10018304]
Glaucoma secondary [MedDRA:10018304]
Glaucoma steroid-induced [MedDRA:10018304]
Glaucoma with increased episcleral venous pressure [MedDRA:10018304]
Glaucoma, unspecified [MedDRA:10018304]
Other specified forms of glaucoma [MedDRA:10018304]
Other specified glaucoma [MedDRA:10018304]
Secondary glaucoma [MedDRA:10018304]
Unspecified glaucoma [MedDRA:10018304]
Glaucoma aggravated [MedDRA:10018304]
Neovascular glaucoma [MedDRA:10018304]
Lens induced glaucoma [MedDRA:10018304]
Lens particle glaucoma [MedDRA:10018304]
Glaucoma (50% of males) [OMIM:Glaucoma (50% of males)]
Glaucoma (75%) [OMIM:Glaucoma (75%)]
Glaucoma (in 80% of patients) [OMIM:Glaucoma (in 80% of patients)]
Glaucoma (in some patients) [OMIM:Glaucoma (in some patients)]
Glaucoma (rare) [OMIM:Glaucoma (rare)]
Glaucoma (uncommon) [OMIM:Glaucoma (uncommon)]
Glaucoma, secondary [OMIM:Glaucoma, secondary]
Neovascular glaucoma [OMIM:Neovascular glaucoma]
Secondary glaucoma [OMIM:Secondary glaucoma]
Glaucomas (excl congenital) [MedDRA:10018305]
Quality:
Cross references:
HPO:0007906 "Increased intraocular pressure" [Orphanet:4040]
Orphanet:4040 "Glaucoma" [Orphanet:4040]
OMIM: "Glaucoma" [OMIM:Glaucoma]
OMIM: "Glaucoma (50% of males)" [OMIM:Glaucoma (50% of males)]
OMIM: "Glaucoma (75%)" [OMIM:Glaucoma (75%)]
OMIM: "Glaucoma (in 80% of patients)" [OMIM:Glaucoma (in 80% of patients)]
OMIM: "Glaucoma (in some patients)" [OMIM:Glaucoma (in some patients)]
OMIM: "Glaucoma (rare)" [OMIM:Glaucoma (rare)]
OMIM: "Glaucoma (uncommon)" [OMIM:Glaucoma (uncommon)]
OMIM: "Glaucoma, secondary" [OMIM:Glaucoma, secondary]
OMIM: "Neovascular glaucoma" [OMIM:Neovascular glaucoma]
OMIM: "Secondary glaucoma" [OMIM:Secondary glaucoma]
UMLS:C1962986 "Glaucoma" [HPO:0000501]
UMLS:C0017601 "Glaucoma" [Orphanet:4040]
UMLS:C0234708 "Raised intraocular pressure" [Orphanet:4040]
Is a (Direct Parents):
HPO         Abnormal eye physiology
Orphanet Abnormality of the eye
MedDRA Glaucoma and ocular hypertension
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)
MedDRA:
Eye disorders(MedDRA:10015919)
    Glaucoma and ocular hypertension(MedDRA:10018307)
       Glaucoma(HPO:0000501)
Database Frequency: 180 / 7739
Resource:

All diseases associated with this symptom:

17q12 microduplication syndrome (Orphanet:261272)
1q21.1 microduplication syndrome (Orphanet:250994)
3C syndrome (Orphanet:7)
3MC SYNDROME 1 (OMIM:257920)
AXENFELD-RIEGER SYNDROME, TYPE 1 (OMIM:180500)
AXENFELD-RIEGER SYNDROME, TYPE 2 (OMIM:601499)
AXENFELD-RIEGER SYNDROME, TYPE 3 (OMIM:602482)
Ackerman syndrome (Orphanet:2561)
Acromelic frontonasal dysplasia (Orphanet:1827)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Aniridia (Orphanet:77)
Aniridia - absent patella (Orphanet:1069)
Aniridia - renal agenesis - psychomotor retardation (Orphanet:1064)
Antecubital pterygium syndrome (Orphanet:2987)
Autosomal recessive proximal renal tubular acidosis (Orphanet:93607)
Autosomal recessive spastic paraplegia type 45 (Orphanet:320396)
Autosomal recessive spastic paraplegia type 48 (Orphanet:306511)
Axenfeld anomaly (Orphanet:98978)
Axenfeld-Rieger syndrome (Orphanet:782)
Bardet-Biedl syndrome (Orphanet:110)
Blau syndrome (Orphanet:90340)
Blepharoptosis - myopia - ectopia lentis (Orphanet:1259)
Brittle cornea syndrome (Orphanet:90354)
CATARACT 22, MULTIPLE TYPES (OMIM:609741)
CATARACT 42 (OMIM:115900)
CATARACT 9, MULTIPLE TYPES (OMIM:604219)
CHARGE syndrome (Orphanet:138)
CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1 (OMIM:122000)
Camurati-Engelmann disease (Orphanet:1328)
Cataract-congenital heart disease-neural tube defect syndrome (Orphanet:314993)
Cerebroretinal vasculopathy (Orphanet:3421)
Charcot-Marie-Tooth disease type 4B2 (Orphanet:99956)
Chylous ascites (Orphanet:1160)
Classical homocystinuria (Orphanet:394)
Coats disease (Orphanet:190)
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome (Orphanet:1369)
Congenital microcoria (Orphanet:566)
Congenital rubella syndrome (Orphanet:290)
Congenital stromal corneal dystrophy (Orphanet:101068)
Cornelia de Lange syndrome (Orphanet:199)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES (OMIM:127200)
Desbuquois syndrome (Orphanet:1425)
Distal monosomy 6p (Orphanet:96125)
Distal trisomy 14q (Orphanet:1705)
Dyschromatosis universalis hereditaria 1 (OMIM:127500)
Dyschromatosis universalis hereditaria 2 (OMIM:612715)
Dyschromatosis universalis hereditaris 3 (OMIM:615402)
Dyssegmental dysplasia - glaucoma (Orphanet:1804)
Dyssegmental dysplasia, Rolland-Desbuquois type (Orphanet:156731)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 (OMIM:601776)
EXFOLIATION SYNDROME (OMIM:177650)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Ehlers-Danlos syndrome, musculocontractural type (Orphanet:2953)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Erythrokeratodermia variabilis (Orphanet:317)
Familial multiple nevi flammei (Orphanet:624)
Familial vascular leukoencephalopathy (Orphanet:36383)
Fibrodysplasia ossificans progressiva (Orphanet:337)
Fine-Lubinsky syndrome (Orphanet:1272)
Frank-Ter Haar syndrome (Orphanet:137834)
GAPO syndrome (Orphanet:2067)
GLAUCOMA 1, OPEN ANGLE, P (OMIM:177700)
GLAUCOMA WITH ELEVATED EPISCLERAL VENOUS PRESSURE (OMIM:137700)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Glaucoma - sleep apnea (Orphanet:2085)
Glaucoma secondary to spherophakia/ectopia lentis and megalocornea (Orphanet:238763)
Gorlin syndrome (Orphanet:377)
HERNS syndrome (Orphanet:63261)
Hallermann-Streiff syndrome (Orphanet:2108)
Hennekam syndrome (Orphanet:2136)
Hereditary vascular retinopathy (Orphanet:71291)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
IRIDOGONIODYSGENESIS, TYPE 2 (OMIM:137600)
IRIS HYPOPLASIA WITH GLAUCOMA (OMIM:308500)
IRIS PIGMENT LAYER, CLEAVAGE OF (OMIM:147610)
Intellectual deficit, X-linked, Armfield type (Orphanet:85276)
Isolated aniridia (Orphanet:250923)
Isolated anophthalmia - microphthalmia (Orphanet:2542)
Isolated cryptophthalmia (Orphanet:91396)
Isolated ectopia lentis (Orphanet:1885)
Juvenile glaucoma (Orphanet:98977)
Klippel-Trénaunay syndrome (Orphanet:90308)
Kniest dysplasia (Orphanet:485)
Lowry-MacLean syndrome (Orphanet:2409)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III (OMIM:210730)
MICROPHTHALMIA WITH HYPEROPIA, RETINAL DEGENERATION, MACROPHAKIA,AND DENTAL ANOMALIES (OMIM:251700)
MICROPHTHALMIA, ISOLATED 1 (OMIM:251600)
MOMO syndrome (Orphanet:2563)
MRCS syndrome (Orphanet:263347)
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)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 7 (OMIM:614643)
Marfan syndrome (Orphanet:558)
Marfan syndrome type 1 (Orphanet:284963)
Marshall syndrome (Orphanet:560)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Microcephaly - lymphedema - chorioretinopathy (Orphanet:2526)
Microcornea - glaucoma - absent frontal sinuses (Orphanet:2536)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Microphthalmia, Lenz type (Orphanet:568)
Mitochondrial myopathy and sideroblastic anemia (Orphanet:2598)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Muckle-Wells syndrome (Orphanet:575)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 6 (Orphanet:583)
Muscle-eye-brain disease (Orphanet:588)
Nail-patella syndrome (Orphanet:2614)
Nance-Horan syndrome (Orphanet:627)
Nanophthalmia (Orphanet:35612)
Neurofibromatosis type 1 (Orphanet:636)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)
Norrie disease (Orphanet:649)
OCULODENTODIGITAL DYSPLASIA (OMIM:164200)
OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY (OMIM:212550)
Oculo-palato-cerebral syndrome (Orphanet:2714)
Oculocerebrorenal syndrome (Orphanet:534)
Oculodentodigital dysplasia (Orphanet:2710)
Oculofaciocardiodental syndrome (Orphanet:2712)
Ophthalmomandibulomelic dysplasia (Orphanet:2741)
Osteogenesis imperfecta (Orphanet:666)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
PHACE syndrome (Orphanet:42775)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 5 (OMIM:613077)
Parkes Weber syndrome (Orphanet:90307)
Peters-plus syndrome (Orphanet:709)
Phakomatosis pigmentovascularis (Orphanet:2875)
Posterior polymorphous corneal dystrophy (Orphanet:98973)
Proteus syndrome (Orphanet:744)
Proximal renal tubular acidosis (Orphanet:47159)
Pseudoprogeria syndrome (Orphanet:2985)
Retinal degeneration - nanophthalmos - glaucoma (Orphanet:1574)
Retinal vasculopathy and cerebral leukodystrophy (Orphanet:247691)
Retinitis pigmentosa (Orphanet:791)
Rieger anomaly (Orphanet:91483)
Roberts syndrome (Orphanet:3103)
Rothmund-Thomson syndrome (Orphanet:2909)
Rubinstein-Taybi syndrome (Orphanet:783)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
SARCOIDOSIS, SUSCEPTIBILITY TO, 1 (OMIM:181000)
SHORT syndrome (Orphanet:3163)
SINGLETON-MERTEN SYNDROME 2 (OMIM:616298)
STICKLER SYNDROME, TYPE I (OMIM:108300)
Sarcoidosis (Orphanet:797)
Scheie syndrome (Orphanet:93474)
Seckel syndrome (Orphanet:808)
Short stature - deafness - neutrophil dysfunction - dysmorphism (Orphanet:2866)
Singleton-Merten dysplasia (Orphanet:85191)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Spastic paraplegia - glaucoma - intellectual deficit (Orphanet:2818)
Spondyloepiphyseal dysplasia congenita (Orphanet:94068)
Stickler syndrome (Orphanet:828)
Stickler syndrome type 2 (Orphanet:90654)
Stiff skin syndrome (Orphanet:2833)
Sturge-Weber syndrome (Orphanet:3205)
Subaortic stenosis - short stature (Orphanet:3191)
Trisomy 18 (Orphanet:3380)
Uveal coloboma - cleft lip and palate - intellectual deficit (Orphanet:1473)
Vogt-Koyanagi-Harada disease (Orphanet:3437)
Von Hippel anomaly (Orphanet:98941)
Von Hippel-Lindau disease (Orphanet:892)
WAGR syndrome (Orphanet:893)
WARBURG MICRO SYNDROME 4 (OMIM:615663)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)
WEILL-MARCHESANI-LIKE SYNDROME (OMIM:613195)
Wagner disease (Orphanet:898)
Walker-Warburg syndrome (Orphanet:899)
Weill-Marchesani syndrome (Orphanet:3449)
Williams syndrome (Orphanet:904)
Wolfram syndrome (Orphanet:3463)
Wolfram syndrome 1 (OMIM:222300)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)
X-linked retinoschisis (Orphanet:792)
Zellweger syndrome (Orphanet:912)
[DEL] SENGERS SYNDROME (OMIM:212350)
[DEL] Wolfram-like syndrome, autosomal dominant (OMIM:614296)