Severe Myopia
Symptom Information:
Symptom ID: | HPO:0011003 | |||||||
Synonyms: |
|
|||||||
Quality: | ||||||||
Cross references: |
|
|||||||
Is a (Direct Parents): |
|
|||||||
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) Myopia(HPO:0000545) Severe Myopia(HPO:0011003) MedDRA: |
|||||||
Database Frequency: | 31 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
ACHROMATOPSIA 3 | (OMIM:262300) |
Aplasia cutis - myopia | (Orphanet:1117) |
Autosomal recessive Stickler syndrome | (Orphanet:250984) |
Autosomal recessive deafness-onychodystrophy syndrome | (Orphanet:79500) |
CONE-ROD DYSTROPHY 18 | (OMIM:615374) |
Congenital ichthyosis - intellectual deficit - spastic quadriplegia | (Orphanet:352333) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Donnai-Barrow syndrome | (Orphanet:2143) |
Dwarfism - intellectual deficit - eye abnormality | (Orphanet:2650) |
ECTOPIA LENTIS ET PUPILLAE | (OMIM:225200) |
EPIPHYSEAL DYSPLASIA OF FEMORAL HEAD, MYOPIA, AND DEAFNESS | (OMIM:226950) |
Glaucoma - ectopia - microspherophakia - stiff joints - short stature | (Orphanet:2084) |
High myopia-sensorineural deafness syndrome | (Orphanet:363396) |
Intellectual deficit, X-linked, Snyder type | (Orphanet:3063) |
Knobloch syndrome | (Orphanet:1571) |
Lethal congenital contracture syndrome type 2 | (Orphanet:137776) |
MENTAL RETARDATION, X-LINKED 92 | (OMIM:300851) |
MYOPIA 17, AUTOSOMAL DOMINANT | (OMIM:608367) |
MYOPIA 19, AUTOSOMAL DOMINANT | (OMIM:613969) |
MYOPIA 2, AUTOSOMAL DOMINANT | (OMIM:160700) |
MYOPIA 21, AUTOSOMAL DOMINANT | (OMIM:614167) |
MYOPIA 23, AUTOSOMAL RECESSIVE | (OMIM:615431) |
MYOPIA 3, AUTOSOMAL DOMINANT | (OMIM:603221) |
MYOPIA 5, AUTOSOMAL DOMINANT | (OMIM:608474) |
MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION | (OMIM:614292) |
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A | (OMIM:310500) |
STICKLER SYNDROME, TYPE V | (OMIM:614284) |
Sinus node disease and myopia | (OMIM:182190) |
WEILL-MARCHESANI SYNDROME 1 | (OMIM:277600) |
Weill-Marchesani syndrome | (Orphanet:3449) |
X-linked cone dysfunction syndrome with myopia | (Orphanet:90001) |