Long palpebral fissure

Symptom Information:

Symptom ID: HPO:0000637
Synonyms:
Long palpebral fissures [HPO:0000637]
Wide palpebral fissure [HPO:0000637]
Wide palpebral fissures [HPO:0000637]
Euryblepharon (disorder) [Orphanet:7600]
Congenital euryblepharon [Orphanet:7600]
Long palpebral fissure [OMIM:Long palpebral fissure]
Long palpebral fissures [OMIM:Long palpebral fissures]
Wide palpebral fissures [OMIM:Wide palpebral fissures]
Euryblepharon/wide palpebral fissures [Orphanet:7600]
Wide palpebral fissures (34%) [OMIM:Wide palpebral fissures (34%)]
Wide palpebral fissures (50%) [OMIM:Wide palpebral fissures (50%)]
Wide palpebral fissures (in some patients) [OMIM:Wide palpebral fissures (in some patients)]
Quality:
Cross references:
Orphanet:7600 "Euryblepharon/wide palpebral fissures" [Orphanet:7600]
OMIM: "Long palpebral fissure" [OMIM:Long palpebral fissure]
OMIM: "Long palpebral fissures" [OMIM:Long palpebral fissures]
OMIM: "Wide palpebral fissures" [OMIM:Wide palpebral fissures]
OMIM: "Wide palpebral fissures (34%)" [OMIM:Wide palpebral fissures (34%)]
OMIM: "Wide palpebral fissures (50%)" [OMIM:Wide palpebral fissures (50%)]
OMIM: "Wide palpebral fissures (in some patients)" [OMIM:Wide palpebral fissures (in some patients)]
UMLS:C1303001 "Congenital euryblepharon" [Orphanet:7600]
Is a (Direct Parents):
HPO         Abnormal size of the palpebral fissures
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)
                      Abnormality of the palpebral fissures(HPO:0008050)
                         Abnormal size of the palpebral fissures(HPO:0200007)
                            Long palpebral fissure(HPO:0000637)
                Abnormality of the periorbital region(HPO:0000606)
                   Abnormality of the eyelid(HPO:0000492)
                      Abnormality of the palpebral fissures(HPO:0008050)
                         Abnormal size of the palpebral fissures(HPO:0200007)
                            Long palpebral fissure(HPO:0000637)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
BARAITSER-WINTER SYNDROME 2 (OMIM:614583)
Baraitser-Winter syndrome (Orphanet:2995)
CHROMOSOME 5q12 DELETION SYNDROME (OMIM:615668)
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY (OMIM:600906)
FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS (OMIM:227255)
Familial intestinal malrotation - facial anomalies (Orphanet:2454)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 (OMIM:239300)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2 (OMIM:614749)
Hyperphosphatasia-intellectual deficiency syndrome (Orphanet:247262)
KABUKI SYNDROME 1 (OMIM:147920)
KABUKI SYNDROME 2 (OMIM:300867)
KBG syndrome (Orphanet:2332)
Kabuki syndrome (Orphanet:2322)
Mandibulofacial dysostosis - macroblepharon - macrostomia (Orphanet:357158)
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus (Orphanet:83473)
OSTEOGENESIS IMPERFECTA, TYPE XIII (OMIM:614856)
PONTOCEREBELLAR HYPOPLASIA, TYPE 10 (OMIM:615803)
Pontocerebellar hypoplasia type 3 (Orphanet:97249)