Aplasia/Hypoplasia of the lens

Symptom Information:

Symptom ID: HPO:0008063
Synonyms:
Microphakia [Orphanet:4740]
Microphakia (disorder) [Orphanet:4740]
Aphakia/microphakia/spherophakia/biphakia/absence of lens/lenticone/lentiglobus [Orphanet:4740]
Biphakia [Orphanet:4740]
Spherophakia [MedDRA:10041513]
Spherophakia (disorder) [Orphanet:4740]
Spherophakia [Orphanet:4740]
Spherophakia [OMIM:Spherophakia]
Aphakia [MedDRA:10002945]
Aphakia (disorder) [Orphanet:4740]
Aphakia [Orphanet:4740]
Quality:
Cross references:
Orphanet:4740 "Aphakia/microphakia/spherophakia/biphakia/absence of lens/lenticone/lentiglobus" [Orphanet:4740]
OMIM: "Spherophakia" [OMIM:Spherophakia]
UMLS:C0266541 "Microphakia" [Orphanet:4740]
UMLS:C0266542 "Spherophakia" [Orphanet:4740]
UMLS:C0003534 "Aphakia" [Orphanet:4740]
Is a (Direct Parents):
Orphanet Lenticonus
Orphanet Abnormality of the eye
HPO         Abnormality of the lens
HPO         Aplasia/Hypoplasia affecting the anterior segment of the eye
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)
                Aplasia/Hypoplasia affecting the eye(HPO:0008056)
                   Aplasia/Hypoplasia affecting the anterior segment of the eye(HPO:0008062)
                      Aplasia/Hypoplasia of the lens(HPO:0008063)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the lens(HPO:0000517)
                      Aplasia/Hypoplasia of the lens(HPO:0008063)
                   Aplasia/Hypoplasia affecting the anterior segment of the eye(HPO:0008062)
                      Aplasia/Hypoplasia of the lens(HPO:0008063)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A (Orphanet:308386)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B (Orphanet:308393)
WEILL-MARCHESANI-LIKE SYNDROME (OMIM:613195)