Abnormality of the anterior chamber
Symptom Information:
Symptom ID: | HPO:0000593 | ||||||||||||||
Synonyms: |
|
||||||||||||||
Quality: | |||||||||||||||
Cross references: |
|
||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the eye(HPO:0000478) Abnormal eye morphology(HPO:0012372) Abnormality of the globe(HPO:0012374) Abnormality of the anterior segment of the globe(HPO:0004328) Abnormality of the anterior chamber(HPO:0000593) MedDRA: Eye disorders(MedDRA:10015919) Congenital eye disorders (excl glaucoma)(MedDRA:10010463) Congenital anterior segment disorders(MedDRA:10010366) Abnormality of the anterior chamber(HPO:0000593) |
||||||||||||||
Database Frequency: | 15 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
3MC SYNDROME 1 | (OMIM:257920) |
Alagille syndrome due to 20p12 microdeletion | (Orphanet:261600) |
Alagille syndrome due to a JAG1 point mutation | (Orphanet:261619) |
Axenfeld-Rieger syndrome | (Orphanet:782) |
Bohring-Opitz syndrome | (Orphanet:97297) |
Coats disease | (Orphanet:190) |
Distal monosomy 6p | (Orphanet:96125) |
Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
Encephalocraniocutaneous lipomatosis | (Orphanet:2396) |
Juvenile xanthogranuloma | (Orphanet:158000) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Peters-plus syndrome | (Orphanet:709) |
Ramon syndrome | (Orphanet:3019) |
SHORT syndrome | (Orphanet:3163) |
Tietz syndrome | (Orphanet:42665) |