Hypermetropia

Symptom Information:

Symptom ID: HPO:0000540
Synonyms:
Farsightedness [HPO:0000540]
Hyperopia [HPO:0000540]
Long-sightedness. [HPO:0000540]
Hypermetropia (disorder) [Orphanet:5600]
Hyperopia [Orphanet:5600]
Hypermetropia [OMIM:Hypermetropia]
Hyperopia [OMIM:Hyperopia]
Hypermetropia [Orphanet:5600]
Hypermetropia [MedDRA:10020675]
Hyperopia [MedDRA:10020675]
Long-sighted [MedDRA:10020675]
Farsighted [MedDRA:10020675]
Hypermetropia (1 patient) [OMIM:Hypermetropia (1 patient)]
Hypermetropia (36%) [OMIM:Hypermetropia (36%)]
Hypermetropia (MEB) [OMIM:Hypermetropia (MEB)]
Hypermetropia (farsightedness) [OMIM:Hypermetropia (farsightedness)]
Hypermetropia (in some patients) [OMIM:Hypermetropia (in some patients)]
Hypermetropia (rare) [OMIM:Hypermetropia (rare)]
Hyperopia (in some patients) [OMIM:Hyperopia (in some patients)]
Quality:
Cross references:
HPO:0008499 "High-grade hypermetropia" [Orphanet:5600]
Orphanet:5600 "Hypermetropia" [Orphanet:5600]
OMIM: "Hypermetropia" [OMIM:Hypermetropia]
OMIM: "Hyperopia" [OMIM:Hyperopia]
OMIM: "Hypermetropia (1 patient)" [OMIM:Hypermetropia (1 patient)]
OMIM: "Hypermetropia (36%)" [OMIM:Hypermetropia (36%)]
OMIM: "Hypermetropia (MEB)" [OMIM:Hypermetropia (MEB)]
OMIM: "Hypermetropia (farsightedness)" [OMIM:Hypermetropia (farsightedness)]
OMIM: "Hypermetropia (in some patients)" [OMIM:Hypermetropia (in some patients)]
OMIM: "Hypermetropia (rare)" [OMIM:Hypermetropia (rare)]
OMIM: "Hyperopia (in some patients)" [OMIM:Hyperopia (in some patients)]
UMLS:C0020490 "Hypermetropia" [HPO:0000540]
UMLS:C0020490 "Hyperopia" [Orphanet:5600]
Is a (Direct Parents):
MedDRA Refractive and accommodative disorders
HPO         Abnormality of refraction
Orphanet Abnormality of the eye
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Abnormality of refraction(HPO:0000539)
                Hypermetropia(HPO:0000540)
MedDRA:
Eye disorders(MedDRA:10015919)
    Vision disorders(MedDRA:10047518)
       Refractive and accommodative disorders(MedDRA:10038267)
          Hypermetropia(HPO:0000540)
Database Frequency: 99 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
17p11.2 microduplication syndrome (Orphanet:1713)
17q12 microdeletion syndrome (Orphanet:261265)
1p36 deletion syndrome (Orphanet:1606)
1q21.1 microdeletion syndrome (Orphanet:250989)
2q23.1 microdeletion syndrome (Orphanet:228402)
AARSKOG-SCOTT SYNDROME (OMIM:305400)
ASYMMETRIC SHORT STATURE SYNDROME (OMIM:108450)
Acro-osteolysis-keloid-like lesions-premature aging syndrome (Orphanet:363665)
Alpha-mannosidosis (Orphanet:61)
Alström syndrome (Orphanet:64)
Amaurosis - hypertrichosis (Orphanet:1021)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Autosomal dominant Kenny-Caffey syndrome (Orphanet:93325)
Autosomal dominant brachyolmia (Orphanet:93304)
Autosomal dominant nonsyndromic intellectual deficit (Orphanet:178469)
Autosomal recessive spastic paraplegia type 45 (Orphanet:320396)
Blepharophimosis - epicanthus inversus - ptosis (Orphanet:126)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Brachydactyly type B2 (Orphanet:140908)
Brachyolmia (Orphanet:1293)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME B (OMIM:133540)
CORNEA PLANA 2 (OMIM:217300)
Cartilage-hair hypoplasia (Orphanet:175)
Cataract - aberrant oral frenula - growth delay (Orphanet:1373)
Cataract-congenital heart disease-neural tube defect syndrome (Orphanet:314993)
Caudal appendage - deafness (Orphanet:1123)
Cockayne syndrome (Orphanet:191)
Costello syndrome (Orphanet:3071)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 4 (OMIM:614378)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Cystoid macular dystrophy (Orphanet:75381)
DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES (OMIM:127200)
Deaf blind hypopigmentation syndrome, Yemenite type (Orphanet:3214)
Deafness with labyrinthine aplasia, microtia, and microdontia (Orphanet:90024)
Distal monosomy 6p (Orphanet:96125)
Dubowitz syndrome (Orphanet:235)
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis (Orphanet:31043)
Familial vascular leukoencephalopathy (Orphanet:36383)
Floating-Harbor syndrome (Orphanet:2044)
Glaucoma secondary to spherophakia/ectopia lentis and megalocornea (Orphanet:238763)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
HELSMOORTEL-VAN DER AA SYNDROME (OMIM:615873)
Hurler-Scheie syndrome (Orphanet:93476)
Intellectual deficit, X-linked - seizures - psoriasis (Orphanet:3052)
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome (Orphanet:363611)
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome (Orphanet:369837)
Isolated ectopia lentis (Orphanet:1885)
Kenny-Caffey syndrome (Orphanet:2333)
Koolen-De Vries syndrome (Orphanet:96169)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Leber congenital amaurosis 10 (OMIM:611755)
Leber congenital amaurosis 15 (OMIM:613843)
Leber congenital amaurosis 5 (OMIM:604537)
Leber congenital amaurosis 9 (OMIM:608553)
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS (OMIM:613671)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III (OMIM:210730)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 (OMIM:613150)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 (OMIM:253800)
Macular coloboma - cleft palate - hallux valgus (Orphanet:91494)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Microphthalmia - retinitis pigmentosa - foveoschisis - optic disc drusen (Orphanet:251279)
Mulibrey nanism (Orphanet:2576)
Myhre syndrome (Orphanet:2588)
Nanophthalmia (Orphanet:35612)
Nijmegen breakage syndrome-like disorder (Orphanet:240760)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Ocular albinism with congenital sensorineural deafness (Orphanet:352740)
Oculocutaneous albinism (Orphanet:55)
Oculodentodigital dysplasia (Orphanet:2710)
Pigmented paravenous retinochoroidal atrophy (Orphanet:251295)
Pilodental dysplasia - refractive errors (Orphanet:2892)
Pontocerebellar hypoplasia type 8 (Orphanet:324569)
Posterior amorphous corneal dystrophy (Orphanet:98971)
Prader-Willi syndrome (Orphanet:739)
Primordial short stature - microdontia - opalescent and rootless teeth (Orphanet:46658)
RETINOPATHY, PERICENTRAL PIGMENTARY, AUTOSOMAL RECESSIVE (OMIM:268060)
RETINOSCHISIS OF FOVEA (OMIM:268080)
Renpenning syndrome (Orphanet:3242)
Retinopathy, Burgess-Black type (Orphanet:139455)
Roifman syndrome (Orphanet:353298)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
SOTOS SYNDROME 1 (OMIM:117550)
Short stature - craniofacial anomalies - genital hypoplasia (Orphanet:2994)
Sotos syndrome (Orphanet:821)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Stapes ankylosis with broad thumbs and toes (Orphanet:140917)
Syndromic X-linked intellectual deficit due to JARID1C mutation (Orphanet:85279)
Thoracolaryngopelvic dysplasia (Orphanet:3317)
Trichodermodysplasia - dental alterations (Orphanet:3353)
Usher syndrome (Orphanet:886)
Usher syndrome type 1 (Orphanet:231169)
Usher syndrome type 3 (Orphanet:231183)
Williams syndrome (Orphanet:904)
X-linked creatine transporter deficiency (Orphanet:52503)
X-linked retinoschisis (Orphanet:792)