RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 7
OrphanetNr:
OMIM Id: 616108
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0000687) Widely spaced teeth 40 / 7739
2
 (HPO:0000689) Dental malocclusion 114 / 7739
3
 (HPO:0000272) Malar flattening 277 / 7739
4
 (HPO:0000582) Upslanted palpebral fissure 185 / 7739
5
 (HPO:0000556) Retinal dystrophy 65 / 7739
6
 (HPO:0001263) Global developmental delay 853 / 7739
7
 (HPO:0004322) Short stature 1232 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: