Upper eyelid coloboma

Symptom Information:

Symptom ID: HPO:0000636
Synonyms:
Upper eyelid colobomas [HPO:0000636]
Upper eyelid coloboma [OMIM:Upper eyelid coloboma]
Upper eyelid colobomas [OMIM:Upper eyelid colobomas]
Quality:
Cross references:
OMIM: "Upper eyelid coloboma" [OMIM:Upper eyelid coloboma]
OMIM: "Upper eyelid colobomas" [OMIM:Upper eyelid colobomas]
Is a (Direct Parents):
HPO         Cleft 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)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of the eyelid(HPO:0000492)
                      Cleft eyelid(HPO:0000625)
                         Upper eyelid coloboma(HPO:0000636)
                Abnormality of the periorbital region(HPO:0000606)
                   Abnormality of the eyelid(HPO:0000492)
                      Cleft eyelid(HPO:0000625)
                         Upper eyelid coloboma(HPO:0000636)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Coloboma(HPO:0000589)
                Cleft eyelid(HPO:0000625)
                   Upper eyelid coloboma(HPO:0000636)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Fraser syndrome (Orphanet:2052)
Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome (Orphanet:306542)
Goldenhar syndrome (Orphanet:374)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Hypospadias - hypertelorism - coloboma and deafness (Orphanet:157788)
Nasopalpebral lipoma - coloboma - telecanthus (Orphanet:2399)
Treacher-Collins syndrome (Orphanet:861)