Iris atrophy

Symptom Information:

Symptom ID: HPO:0001089
Synonyms:
Iris hypoplasia [Orphanet:4160]
Aniridia [Orphanet:4160]
Hypoplasia of iris (disorder) [Orphanet:4160]
Congenital aniridia (disorder) [Orphanet:4160]
Hypoplasia of iris [Orphanet:4160]
Iris atrophy [OMIM:Iris atrophy]
Aniridia/iris hypoplasia [Orphanet:4160]
Hypoplastic iris [Orphanet:4160]
Iris atrophy [MedDRA:10022948]
Degeneration of pupillary margin [MedDRA:10022948]
Degenerations of iris and ciliary body [MedDRA:10022948]
Essential or progressive iris atrophy [MedDRA:10022948]
Miotic cysts of pupillary margin [MedDRA:10022948]
Other iris atrophy [MedDRA:10022948]
Pigmentary iris degeneration [MedDRA:10022948]
Iris degeneration [MedDRA:10022948]
Hypoplastic iris [MedDRA:10022948]
Aniridia [MedDRA:10002532]
Anirida [MedDRA:10002532]
Aniridia (3%) [OMIM:Aniridia (3%)]
Hypoplastic irides [OMIM:Hypoplastic irides]
Iris hypoplasia (reported in 1 family) [OMIM:Iris hypoplasia (reported in 1 family)]
Quality:
Cross references:
HPO:0008053 "Aplasia/Hypoplasia of the iris" [Orphanet:4160]
HPO:0007676 "Hypoplasia of the iris" [Orphanet:4160]
HPO:0007990 "Hypoplastic iris stroma" [Orphanet:4160]
HPO:0000526 "Aniridia" [Orphanet:4160]
Orphanet:4160 "Aniridia/iris hypoplasia" [Orphanet:4160]
OMIM: "Iris atrophy" [OMIM:Iris atrophy]
OMIM: "Aniridia (3%)" [OMIM:Aniridia (3%)]
OMIM: "Hypoplastic irides" [OMIM:Hypoplastic irides]
OMIM: "Iris hypoplasia (reported in 1 family)" [OMIM:Iris hypoplasia (reported in 1 family)]
UMLS:C0344539 "Hypoplasia of iris" [Orphanet:4160]
UMLS:C0003076 "Aniridia" [Orphanet:4160]
Is a (Direct Parents):
MedDRA Iris and choroid disorders congenital
HPO         Abnormality of the iris
Orphanet Abnormality of the eye
MedDRA Iris and ciliary body structural change, deposit and degeneration
Orphanet Aniridia
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 uvea(HPO:0000553)
                   Abnormality of the iris(HPO:0000525)
                      Iris atrophy(HPO:0001089)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the iris(HPO:0000525)
                      Iris atrophy(HPO:0001089)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Eye disorders congenital(MedDRA:10015920)
       Iris and choroid disorders congenital(MedDRA:10022946)
          Iris atrophy(HPO:0001089)
Eye disorders(MedDRA:10015919)
    Anterior eye structural change, deposit and degeneration(MedDRA:10002693)
       Iris and ciliary body structural change, deposit and degeneration(MedDRA:10022952)
          Iris atrophy(HPO:0001089)
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Acro-fronto-facio-nasal dysostosis (Orphanet:1784)
FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES,AND SPONTANEOUS FILTERING BLEBS (OMIM:601552)
Familial cutaneous collagenoma (Orphanet:53296)
Familial vascular leukoencephalopathy (Orphanet:36383)
Focal dermal hypoplasia (Orphanet:2092)
Multiple system atrophy (Orphanet:102)
Osteoporosis - pseudoglioma (Orphanet:2788)
WAARDENBURG SYNDROME, TYPE 2E (OMIM:611584)