GLAUCOMA 3, PRIMARY INFANTILE, B

General Information (adopted from Orphanet):

Synonyms, Signs: GLC3, TYPE B
GLAUCOMA, PRIMARY CONGENITAL, TYPE B
GLC3B
Number of Symptoms 2
OrphanetNr:
OMIM Id: 600975
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

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

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0008007) Primary congenital glaucoma 2 / 7739
2
 (HPO:0000007) Autosomal recessive inheritance 2538 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: