Ankyloblepharon

Symptom Information:

Symptom ID: HPO:0009755
Synonyms:
Ankyloblepharon filiforme adnatum [HPO:0009755]
Eyelid synechiae [HPO:0009755]
Symblepharon (disorder) [Orphanet:7050]
Ankyloblepharon (disorder) [Orphanet:7050]
Symblepharon [Orphanet:7050]
Ankyloblepharon [Orphanet:7050]
Ankyloblepharon [OMIM:Ankyloblepharon]
Ankyloblepharon filiforme adnatum [OMIM:Ankyloblepharon filiforme adnatum]
Cryptophthalmia/ankyloblepharon/synblepharon [Orphanet:7050]
Symblepharon [MedDRA:10042736]
Symblepharon (adhesion of the eyelid to the eyeball) [OMIM:Symblepharon (adhesion of the eyelid to the eyeball)]
Quality:
Cross references:
Orphanet:7050 "Cryptophthalmia/ankyloblepharon/synblepharon" [Orphanet:7050]
OMIM: "Ankyloblepharon" [OMIM:Ankyloblepharon]
OMIM: "Ankyloblepharon filiforme adnatum" [OMIM:Ankyloblepharon filiforme adnatum]
OMIM: "Symblepharon (adhesion of the eyelid to the eyeball)" [OMIM:Symblepharon (adhesion of the eyelid to the eyeball)]
UMLS:C0339182 "Ankyloblepharon" [HPO:0009755]
UMLS:C0152454 "Symblepharon" [Orphanet:7050]
UMLS:C0339182 "Ankyloblepharon" [Orphanet:7050]
Is a (Direct Parents):
Orphanet Cryptophthalmos
MedDRA Conjunctival structural change, deposit and degeneration
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)
                Abnormality of the periorbital region(HPO:0000606)
                   Abnormality of the eyelid(HPO:0000492)
                      Ankyloblepharon(HPO:0009755)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of the eyelid(HPO:0000492)
                      Ankyloblepharon(HPO:0009755)
MedDRA:
Eye disorders(MedDRA:10015919)
    Anterior eye structural change, deposit and degeneration(MedDRA:10002693)
       Conjunctival structural change, deposit and degeneration(MedDRA:10010735)
          Ankyloblepharon(HPO:0009755)
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Ankyloblepharon filiforme adnatum - cleft palate (Orphanet:1072)
Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)
Bartsocas-Papas syndrome (Orphanet:1234)
CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III (OMIM:611929)
CHANDS (OMIM:214350)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Isolated cryptophthalmia (Orphanet:91396)
MICROPHTHALMIA, ISOLATED 3 (OMIM:611038)
Microphthalmia - ankyloblepharon - intellectual deficit (Orphanet:85275)