Congenital nuclear cataract

Symptom Information:

Symptom ID: HPO:0008024
Synonyms:
Cataract, congenital nuclear [OMIM:Cataract, congenital nuclear]
Congenital nuclear cataract (in some patients) [OMIM:Congenital nuclear cataract (in some patients)]
Quality:
Cross references:
OMIM: "Cataract, congenital nuclear" [OMIM:Cataract, congenital nuclear]
OMIM: "Congenital nuclear cataract (in some patients)" [OMIM:Congenital nuclear cataract (in some patients)]
Is a (Direct Parents):
HPO         Nuclear cataract
HPO         Congenital cataract
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the lens(HPO:0000517)
                      Cataract(HPO:0000518)
                         Zonular cataract(HPO:0010920)
                            Nuclear cataract(HPO:0100018)
                               Congenital nuclear cataract(HPO:0008024)
                         Congenital cataract(HPO:0000519)
                            Congenital nuclear cataract(HPO:0008024)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

CATARACT 2, MULTIPLE TYPES (OMIM:604307)
CATARACT 40 (OMIM:302200)
CATARACT 41 (OMIM:116400)
Hereditary hyperferritinemia with congenital cataracts (Orphanet:163)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)