High-grade hypermetropia
Symptom Information:
Symptom ID: | HPO:0008499 | |||||||||||||||
Synonyms: |
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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) High-grade hypermetropia(HPO:0008499) MedDRA: Eye disorders(MedDRA:10015919) Vision disorders(MedDRA:10047518) Refractive and accommodative disorders(MedDRA:10038267) High-grade hypermetropia(HPO:0008499) |
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Database Frequency: | 14 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
Floating-Harbor syndrome | (Orphanet:2044) |
Glaucoma secondary to spherophakia/ectopia lentis and megalocornea | (Orphanet:238763) |
HYPEROPIA, HIGH | (OMIM:238950) |
Isolated anophthalmia - microphthalmia | (Orphanet:2542) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Leber congenital amaurosis 15 | (OMIM:613843) |
Leber congenital amaurosis 6 | (OMIM:613826) |
Leber congenital amaurosis 8 | (OMIM:613835) |
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS | (OMIM:613671) |
MICROPHTHALMIA WITH HYPEROPIA, RETINAL DEGENERATION, MACROPHAKIA,AND DENTAL ANOMALIES | (OMIM:251700) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 | (OMIM:613150) |
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY | (OMIM:614800) |
X-linked retinoschisis | (Orphanet:792) |