Long palpebral fissure
Symptom Information:
Symptom ID: | HPO:0000637 | ||||||||||||
Synonyms: |
|
||||||||||||
Quality: | |||||||||||||
Cross references: |
|
||||||||||||
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) Abnormality of the palpebral fissures(HPO:0008050) Abnormal size of the palpebral fissures(HPO:0200007) Long palpebral fissure(HPO:0000637) 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) 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) |