Entropion
Symptom Information:
Symptom ID: | HPO:0000621 | ||||||||||||
Synonyms: |
|
||||||||||||
Quality: | |||||||||||||
Cross references: |
|
||||||||||||
Is a (Direct Parents): |
|
||||||||||||
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) |