Entropion

Symptom Information:

Symptom ID: HPO:0000621
Synonyms:
Entropion (disorder) [Orphanet:7400]
Entropion [Orphanet:7400]
Entropion [OMIM:Entropion]
Ectropion/entropion/eyelid eversion [Orphanet:7400]
Entropion [MedDRA:10061842]
Cicatricial entropion [MedDRA:10061842]
Entropion and trichiasis of eyelid [MedDRA:10061842]
Entropion NOS [MedDRA:10061842]
Entropion, unspecified [MedDRA:10061842]
Mechanical entropion [MedDRA:10061842]
Senile entropion [MedDRA:10061842]
Spastic entropion [MedDRA:10061842]
Quality:
Cross references:
Orphanet:7400 "Ectropion/entropion/eyelid eversion" [Orphanet:7400]
OMIM: "Entropion" [OMIM:Entropion]
UMLS:C0014390 "Entropion" [HPO:0000621]
UMLS:C0014390 "Entropion" [Orphanet:7400]
Is a (Direct Parents):
HPO         Abnormality of the eyelid
MedDRA Skin and subcutaneous malformations and anomalies NEC
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)
                      Entropion(HPO:0000621)
                Abnormality of the periorbital region(HPO:0000606)
                   Abnormality of the eyelid(HPO:0000492)
                      Entropion(HPO:0000621)
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)
          Entropion(HPO:0000621)
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

DE SANCTIS-CACCHIONE SYNDROME (OMIM:278800)
ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVEFACIAL FEATURES (OMIM:609944)
Lethal restrictive dermopathy (Orphanet:1662)
SENER SYNDROME (OMIM:606156)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
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)