Severe Myopia

Symptom Information:

Symptom ID: HPO:0011003
Synonyms:
High myopia [HPO:0011003]
Severe myopia (> -6.00 diopters) [HPO:0011003]
High myopia [OMIM:High myopia]
Severe myopia [OMIM:Severe myopia]
High myopia (1 patient) [OMIM:High myopia (1 patient)]
High myopia (in some patients) [OMIM:High myopia (in some patients)]
Severe myopia (> -6.00 diopters) [OMIM:Severe myopia (> -6.00 diopters)]
Quality:
Cross references:
OMIM: "High myopia" [OMIM:High myopia]
OMIM: "Severe myopia" [OMIM:Severe myopia]
OMIM: "High myopia (1 patient)" [OMIM:High myopia (1 patient)]
OMIM: "High myopia (in some patients)" [OMIM:High myopia (in some patients)]
OMIM: "Severe myopia (> -6.00 diopters)" [OMIM:Severe myopia (> -6.00 diopters)]
Is a (Direct Parents):
HPO         Myopia
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)