Anterior pyramidal cataract
Symptom Information:
Symptom ID: | HPO:0010697 | ||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |