Ectropion
Symptom Information:
Symptom ID: | HPO:0000656 | |||||||||||||||
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 head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the periorbital region(HPO:0000606) Abnormality of the eyelid(HPO:0000492) Ectropion(HPO:0000656) obsolete Abnormality of the ocular region(HPO:0000284) Abnormality of the eyelid(HPO:0000492) Ectropion(HPO:0000656) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin and subcutaneous tissue disorders NEC(MedDRA:10040790) Skin and subcutaneous malformations and anomalies NEC(MedDRA:10040889) Ectropion(HPO:0000656) |
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Database Frequency: | 25 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
Barber-Say syndrome | (Orphanet:1231) |
Bathing suit ichthyosis | (Orphanet:100976) |
Craniosynostosis - anal anomalies - porokeratosis | (Orphanet:85199) |
DE SANCTIS-CACCHIONE SYNDROME | (OMIM:278800) |
Dorfman-Chanarin disease | (Orphanet:98907) |
Fetal Gaucher disease | (Orphanet:85212) |
Gaucher disease type 2 | (Orphanet:77260) |
Harlequin ichthyosis | (Orphanet:457) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2 | (OMIM:242100) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3 | (OMIM:606545) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A | (OMIM:601277) |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 | (OMIM:612281) |
Ichthyosis - alopecia - eclabion - ectropion - intellectual deficit | (Orphanet:2269) |
Junctional epidermolysis bullosa - pyloric atresia | (Orphanet:79403) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Postaxial acrofacial dysostosis | (Orphanet:246) |
Self-healing collodion baby | (Orphanet:281122) |
Tangier disease | (Orphanet:31150) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
Xeroderma pigmentosum complementation group A | (Orphanet:276249) |
Xeroderma pigmentosum complementation group C | (Orphanet:276255) |
Xeroderma pigmentosum complementation group D | (Orphanet:276258) |
Xeroderma pigmentosum complementation group E | (Orphanet:276261) |
Xeroderma pigmentosum variant | (Orphanet:90342) |
Xeroderma pigmentosum/Cockayne syndrome complex | (Orphanet:220295) |