Ectropion

Symptom Information:

Symptom ID: HPO:0000656
Synonyms:
Ectropion of eyelid (disorder) [Orphanet:7400]
Everted margin (morphologic abnormality) [Orphanet:7400]
Ectropion [Orphanet:7400]
Ectropion [OMIM:Ectropion]
Ectropion/entropion/eyelid eversion [Orphanet:7400]
Ectropion [MedDRA:10014179]
Cicatricial ectropion [MedDRA:10014179]
Ectropion NOS [MedDRA:10014179]
Ectropion, unspecified [MedDRA:10014179]
Extropion [MedDRA:10014179]
Mechanical ectropion [MedDRA:10014179]
Senile ectropion [MedDRA:10014179]
Spastic ectropion [MedDRA:10014179]
Cicatricial ectropion [OMIM:Cicatricial ectropion]
Ectropion (in some patients) [OMIM:Ectropion (in some patients)]
Quality:
Cross references:
Orphanet:7400 "Ectropion/entropion/eyelid eversion" [Orphanet:7400]
OMIM: "Ectropion" [OMIM:Ectropion]
OMIM: "Cicatricial ectropion" [OMIM:Cicatricial ectropion]
OMIM: "Ectropion (in some patients)" [OMIM:Ectropion (in some patients)]
UMLS:C0013592 "Ectropion" [HPO:0000656]
UMLS:C0013592 "Ectropion" [Orphanet:7400]
Is a (Direct Parents):
MedDRA Skin and subcutaneous malformations and anomalies NEC
Orphanet Entropion
HPO         Abnormality of the eyelid
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)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of the eyelid(HPO:0000492)
                      Ectropion(HPO:0000656)
                Abnormality of the periorbital region(HPO:0000606)
                   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)
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)