Ankyloblepharon
Symptom Information:
Symptom ID: | HPO:0009755 | |||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) Ankyloblepharon(HPO:0009755) Abnormality of the periorbital region(HPO:0000606) 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) |
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Database Frequency: | 10 / 7739 | |||||||||||
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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) |