Abnormality of the orbital region
Symptom Information:
| Symptom ID: | HPO:0000315 | ||||||||
| 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 orbital region(HPO:0000315) MedDRA: |
||||||||
| Database Frequency: | 18 / 7739 | ||||||||
| Resource: |
All diseases associated with this symptom:
| Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
| Ankyloblepharon filiforme - imperforate anus | (Orphanet:1074) |
| Ankyloblepharon filiforme adnatum - cleft palate | (Orphanet:1072) |
| Arthrogryposis with oculomotor limitation and electroretinal anomalies | (Orphanet:1154) |
| Autosomal dominant popliteal pterygium syndrome | (Orphanet:1300) |
| Bartsocas-Papas syndrome | (Orphanet:1234) |
| CHARGE syndrome | (Orphanet:138) |
| Dwarfism - intellectual deficit - eye abnormality | (Orphanet:2650) |
| Fraser syndrome | (Orphanet:2052) |
| Microphthalmia - ankyloblepharon - intellectual deficit | (Orphanet:85275) |
| Microphthalmia with brain and digit anomalies | (Orphanet:139471) |
| Microphthalmia, Lenz type | (Orphanet:568) |
| Oculocerebral dysplasia | (Orphanet:2705) |
| Oculotrichoanal syndrome | (Orphanet:2717) |
| Recessive dystrophic epidermolysis bullosa-generalized other | (Orphanet:89842) |
| Spinocerebellar ataxia type 35 | (Orphanet:276193) |
| Xeroderma pigmentosum | (Orphanet:910) |
| Zlotogora-Ogur syndrome | (Orphanet:3253) |