MICROSPHEROPHAKIA WITH HERNIA

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 7
OrphanetNr:
OMIM Id: 157150
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0008019) Superior lens subluxation 1 / 7739
2
 (HPO:0000545) Myopia 286 / 7739
3
 (HPO:0000541) Retinal detachment 87 / 7739
4
 (HPO:0000023) Inguinal hernia 181 / 7739
5
 (OMIM) Microspherophakia 7 / 7739
6
 (OMIM) Upward lens dislocation 1 / 7739
7
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: