Abnormality of the eyelid
Symptom Information:
Symptom ID: | HPO:0000492 | |
Synonyms: |
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Quality: | ||
Cross references: |
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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) Abnormality of the periorbital region(HPO:0000606) Abnormality of the eyelid(HPO:0000492) obsolete Abnormality of the ocular region(HPO:0000284) Abnormality of the eyelid(HPO:0000492) MedDRA: |
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Database Frequency: | 41 / 7739 | |
Resource: |
All diseases associated with this symptom:
AL amyloidosis | (Orphanet:85443) |
Ablepharon macrostomia syndrome | (Orphanet:920) |
Acrofacial dysostosis, Palagonia type | (Orphanet:1787) |
Autosomal recessive cutis laxa type 2 | (Orphanet:90350) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
Barber-Say syndrome | (Orphanet:1231) |
Blepharo-cheilo-odontic syndrome | (Orphanet:1997) |
Cenani-Lenz syndrome | (Orphanet:3258) |
Classical mycosis fungoides | (Orphanet:2584) |
Congenital non-bullous ichthyosiform erythroderma | (Orphanet:79394) |
DIAMOND-BLACKFAN ANEMIA 11 | (OMIM:614900) |
Dystrophic epidermolysis bullosa | (Orphanet:303) |
EEC syndrome | (Orphanet:1896) |
Ectodermal dysplasia - intellectual deficit - central nervous system malformation | (Orphanet:1812) |
Fetal Gaucher disease | (Orphanet:85212) |
Harlequin ichthyosis | (Orphanet:457) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
Ichthyosis - alopecia - eclabion - ectropion - intellectual deficit | (Orphanet:2269) |
Jacobsen syndrome | (Orphanet:2308) |
Junctional epidermolysis bullosa - pyloric atresia | (Orphanet:79403) |
Kabuki syndrome | (Orphanet:2322) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Kindler syndrome | (Orphanet:2908) |
Lamellar ichthyosis | (Orphanet:313) |
Lethal restrictive dermopathy | (Orphanet:1662) |
Lyell syndrome | (Orphanet:537) |
Lymphedema - distichiasis | (Orphanet:33001) |
Multiple non-ossifying fibromatosis | (Orphanet:2029) |
Oculocerebral hypopigmentation syndrome, Cross type | (Orphanet:2719) |
Oculomaxillofacial dysostosis | (Orphanet:1794) |
Postaxial acrofacial dysostosis | (Orphanet:246) |
Primary cutaneous lymphoma | (Orphanet:542) |
Primary localized amyloidosis | (Orphanet:314709) |
Recessive dystrophic epidermolysis bullosa-generalized other | (Orphanet:89842) |
Rombo syndrome | (Orphanet:3110) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Stevens-Johnson syndrome | (Orphanet:36426) |
Sézary syndrome | (Orphanet:3162) |
Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
Xeroderma pigmentosum | (Orphanet:910) |