Glaucoma
Symptom Information:
Symptom ID: | HPO:0000501 | ||||||||||||||||||||||||||||||||||||||||||||||
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) MedDRA: Eye disorders(MedDRA:10015919) Glaucoma and ocular hypertension(MedDRA:10018307) Glaucoma(HPO:0000501) |
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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) |