Cleft eyelid

Symptom Information:

Symptom ID: HPO:0000625
Synonyms:
Eyelid coloboma [HPO:0000625]
Notched eyelid. [HPO:0000625]
Cleft eyelid [OMIM:Cleft eyelid]
Eyelid coloboma [OMIM:Eyelid coloboma]
Coloboma of the eyelid [Orphanet:7300]
Eyelid colobomas [OMIM:Eyelid colobomas]
Eyelid colobomata (in some patients) [OMIM:Eyelid colobomata (in some patients)]
Quality:
Cross references:
Orphanet:7300 "Coloboma of the eyelid" [Orphanet:7300]
OMIM: "Cleft eyelid" [OMIM:Cleft eyelid]
OMIM: "Eyelid coloboma" [OMIM:Eyelid coloboma]
OMIM: "Eyelid colobomas" [OMIM:Eyelid colobomas]
OMIM: "Eyelid colobomata (in some patients)" [OMIM:Eyelid colobomata (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of the eyelid
HPO         Coloboma
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Coloboma(HPO:0000589)
                Cleft eyelid(HPO:0000625)
       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)
                      Cleft eyelid(HPO:0000625)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of the eyelid(HPO:0000492)
                      Cleft eyelid(HPO:0000625)
MedDRA:
Database Frequency: 31 / 7739
Resource:

All diseases associated with this symptom:

Acro-fronto-facio-nasal dysostosis (Orphanet:1784)
Aicardi-Goutières syndrome (Orphanet:51)
Anophthalmia plus syndrome (Orphanet:1104)
Bartsocas-Papas syndrome (Orphanet:1234)
CHARGE syndrome (Orphanet:138)
Constriction rings syndrome (Orphanet:295000)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
FRONTOFACIONASAL DYSPLASIA (OMIM:229400)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Goldenhar syndrome (Orphanet:374)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
HELSMOORTEL-VAN DER AA SYNDROME (OMIM:615873)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Hypospadias - hypertelorism - coloboma and deafness (Orphanet:157788)
Jacobsen syndrome (Orphanet:2308)
MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES (OMIM:607597)
MOMO syndrome (Orphanet:2563)
Microbrachycephaly - ptosis - cleft lip (Orphanet:2511)
Mycophenolate mofetil embryopathy (Orphanet:268249)
Nager syndrome (Orphanet:245)
Nasopalpebral lipoma - coloboma - telecanthus (Orphanet:2399)
Oculoauriculovertebral spectrum with radial defects (Orphanet:2549)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Oculotrichoanal syndrome (Orphanet:2717)
Postaxial acrofacial dysostosis (Orphanet:246)
Roberts syndrome (Orphanet:3103)
Scalp-ear-nipple syndrome (Orphanet:2036)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
Terminal transverse defects of arm (Orphanet:93937)
Toriello-Lacassie-Droste syndrome (Orphanet:3339)
Treacher-Collins syndrome (Orphanet:861)