EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 5
OrphanetNr:
OMIM Id: 615923
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:0000938) Osteopenia 138 / 7739
2
 (HPO:0010055) Broad hallux 56 / 7739
3
 (HPO:0001847) Long hallux 13 / 7739
4
 (HPO:0001166) Arachnodactyly 62 / 7739
5
 (HPO:0002650) Scoliosis 705 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: