Abnormality of the eyelid

Symptom Information:

Symptom ID: HPO:0000492
Synonyms:
Abnormality of the eyelids [HPO:0000492]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Euryblepharon
HPO         obsolete Abnormality of the ocular region
HPO         Abnormality of levator palpebrae superioris
HPO         Symblepharon
HPO         Abnormality of the periorbital region
HPO         Lipomas of upper eyelids
HPO         Microblepharia
HPO         Lagopthalmos
HPO         Accessory 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)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of the eyelid(HPO:0000492)
MedDRA:
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)
S├ęzary syndrome (Orphanet:3162)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Xeroderma pigmentosum (Orphanet:910)