Shallow orbits
Symptom Information:
Symptom ID: | HPO:0000586 | ||||||
Synonyms: |
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Quality: | |||||||
Cross references: |
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Is a (Direct Parents): |
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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 globe location(HPO:0100886) Proptosis(HPO:0000520) Shallow orbits(HPO:0000586) Abnormality of the orbital region(HPO:0000315) Abnormality of globe location(HPO:0100886) Proptosis(HPO:0000520) Shallow orbits(HPO:0000586) Abnormality of the eye(HPO:0000478) Abnormal eye morphology(HPO:0012372) Abnormality of the globe(HPO:0012374) Abnormality of globe location(HPO:0100886) Proptosis(HPO:0000520) Shallow orbits(HPO:0000586) MedDRA: |
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Database Frequency: | 23 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Apert syndrome | (Orphanet:87) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Cole-Carpenter syndrome | (Orphanet:2050) |
Connective tissue disorder due to lysyl hydroxylase-3 deficiency | (Orphanet:300284) |
Crouzon disease | (Orphanet:207) |
Dyssegmental dysplasia, Rolland-Desbuquois type | (Orphanet:156731) |
Fine-Lubinsky syndrome | (Orphanet:1272) |
Glaucoma - ectopia - microspherophakia - stiff joints - short stature | (Orphanet:2084) |
Hurler syndrome | (Orphanet:93473) |
Marshall-Smith syndrome | (Orphanet:561) |
OSTEOGENESIS IMPERFECTA, TYPE X | (OMIM:613848) |
Osteoglophonic dwarfism | (Orphanet:2645) |
Pfeiffer syndrome | (Orphanet:710) |
ROBERTS SYNDROME | (OMIM:268300) |
ROBINOW-SORAUF SYNDROME | (OMIM:180750) |
Roberts syndrome | (Orphanet:3103) |
Saethre-Chotzen syndrome | (Orphanet:794) |
Sakati-Nyhan syndrome | (Orphanet:3128) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
TRICHOHEPATOENTERIC SYNDROME 1 | (OMIM:222470) |
WEILL-MARCHESANI SYNDROME 1 | (OMIM:277600) |
Weill-Marchesani syndrome | (Orphanet:3449) |