Iris atrophy
Symptom Information:
Symptom ID: | HPO:0001089 | ||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||
Quality: | |||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||||||
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) |