Hypermetropia
Symptom Information:
Symptom ID: | HPO:0000540 | |||||||||||||||||||
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) 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) |
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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) |