Epibulbar dermoid

Symptom Information:

Symptom ID: HPO:0001140
Synonyms:
Epibulbar dermoids [HPO:0001140]
Mature cystic teratoma (morphologic abnormality) [Orphanet:4660]
Dermoid Cyst [Orphanet:4660]
Epibulbar dermoid [OMIM:Epibulbar dermoid]
Epibulbar dermoids [OMIM:Epibulbar dermoids]
Conjunctival tumor/epibulbar dermoid [Orphanet:4660]
Dermoid cyst [OMIM:Dermoid cyst]
Dermoid cyst [MedDRA:10012522]
Dermoid sinus [Orphanet:23160]
Mature cystic teratoma (disorder) [Orphanet:23160]
Dermoid Cyst [Orphanet:23160]
Dermoid sinus/dimple/pit (excluding sacral) [Orphanet:23160]
Quality:
Cross references:
Orphanet:4660 "Conjunctival tumor/epibulbar dermoid" [Orphanet:4660]
Orphanet:23160 "Dermoid sinus/dimple/pit (excluding sacral)" [Orphanet:23160]
OMIM: "Epibulbar dermoid" [OMIM:Epibulbar dermoid]
OMIM: "Epibulbar dermoids" [OMIM:Epibulbar dermoids]
OMIM: "Dermoid cyst" [OMIM:Dermoid cyst]
UMLS:C0011649 "Dermoid Cyst" [Orphanet:4660]
UMLS:C0011649 "Dermoid Cyst" [Orphanet:23160]
Is a (Direct Parents):
HPO         Abnormality of the conjunctiva
Orphanet Abnormality of the eye
Orphanet Abnormality of the skin
HPO         Abnormality of the sclera
HPO         Abnormality of the cornea
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 conjunctiva(HPO:0000502)
                Epibulbar dermoid(HPO:0001140)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the sclera(HPO:0000591)
                   Epibulbar dermoid(HPO:0001140)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the cornea(HPO:0000481)
                      Epibulbar dermoid(HPO:0001140)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Axial mesodermal dysplasia spectrum (Orphanet:1834)
Caudal regression sequence (Orphanet:3027)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Familial caudal dysgenesis (Orphanet:1768)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Goldenhar syndrome (Orphanet:374)
Proteus syndrome (Orphanet:744)
Proteus-like syndrome (Orphanet:2969)
Sirenomelia (Orphanet:3169)
Toriello-Lacassie-Droste syndrome (Orphanet:3339)
Townes-Brocks syndrome (Orphanet:857)