Anterior pyramidal cataract

Symptom Information:

Symptom ID: HPO:0010697
Synonyms:
Pyramidal cataract [HPO:0010697]
Cataract [HPO:0010697]
Cataract (21%) [OMIM:Cataract (21%)]
Cataract (28%) [OMIM:Cataract (28%)]
Cataract (Alport syndrome with macrothrombocytopenia) [OMIM:Cataract (Alport syndrome with macrothrombocytopenia)]
Cataract (in 2 brothers) [OMIM:Cataract (in 2 brothers)]
Cataract (in some patients) [OMIM:Cataract (in some patients)]
Cataracts (1 patient) [OMIM:Cataracts (1 patient)]
Cataracts (anterior- subcapsular) [OMIM:Cataracts (anterior- subcapsular)]
Cataracts (e.g. 180380.0016) [OMIM:Cataracts (e.g. 180380.0016)]
Cataracts (in older patients) [OMIM:Cataracts (in older patients)]
Cataracts (in some patients) [OMIM:Cataracts (in some patients)]
Cataracts (later onset) [OMIM:Cataracts (later onset)]
Cataracts (less common) [OMIM:Cataracts (less common)]
Cataracts (rare) [OMIM:Cataracts (rare)]
Cataracts (uncommon) [OMIM:Cataracts (uncommon)]
Quality:
Cross references:
OMIM: "Cataract (21%)" [OMIM:Cataract (21%)]
OMIM: "Cataract (28%)" [OMIM:Cataract (28%)]
OMIM: "Cataract (Alport syndrome with macrothrombocytopenia)" [OMIM:Cataract (Alport syndrome with macrothrombocytopenia)]
OMIM: "Cataract (in 2 brothers)" [OMIM:Cataract (in 2 brothers)]
OMIM: "Cataract (in some patients)" [OMIM:Cataract (in some patients)]
OMIM: "Cataracts (1 patient)" [OMIM:Cataracts (1 patient)]
OMIM: "Cataracts (anterior- subcapsular)" [OMIM:Cataracts (anterior- subcapsular)]
OMIM: "Cataracts (e.g. 180380.0016)" [OMIM:Cataracts (e.g. 180380.0016)]
OMIM: "Cataracts (in older patients)" [OMIM:Cataracts (in older patients)]
OMIM: "Cataracts (in some patients)" [OMIM:Cataracts (in some patients)]
OMIM: "Cataracts (later onset)" [OMIM:Cataracts (later onset)]
OMIM: "Cataracts (less common)" [OMIM:Cataracts (less common)]
OMIM: "Cataracts (rare)" [OMIM:Cataracts (rare)]
OMIM: "Cataracts (uncommon)" [OMIM:Cataracts (uncommon)]
UMLS:C0086543 "Cataract" [HPO:0010697]
Is a (Direct Parents):
HPO         Anterior polar 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)
                         Polar cataract(HPO:0010696)
                            Anterior polar cataract(HPO:0001134)
                               Anterior pyramidal cataract(HPO:0010697)
MedDRA:
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation (Orphanet:324530)
Autosomal recessive limb-girdle muscular dystrophy type 2T (Orphanet:363623)
Autosomal recessive spastic paraplegia type 26 (Orphanet:101006)
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4 (OMIM:615412)
Congenital intrauterine infection-like syndrome (Orphanet:1229)
DERMATITIS, ATOPIC (OMIM:603165)
EPSTEIN SYNDROME (OMIM:153650)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Intellectual deficit, X-linked, Armfield type (Orphanet:85276)
MEDNIK syndrome (Orphanet:171851)
MEGALOCORNEA (OMIM:309300)
MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE) (OMIM:615418)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 14 (OMIM:615351)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies (Orphanet:369897)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 (OMIM:157640)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 (OMIM:609286)
RETINITIS PIGMENTOSA 4 (OMIM:613731)
Renal tubulopathy - encephalopathy - liver failure (Orphanet:254902)
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis (Orphanet:70595)
Spinocerebellar ataxia with epilepsy (Orphanet:254881)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)