Abnormality of the anterior chamber

Symptom Information:

Symptom ID: HPO:0000593
Synonyms:
Anterior chamber anomalies [HPO:0000593]
Ocular anterior chamber abnormality [HPO:0000593]
Anterior chamber anomaly [Orphanet:4140]
Congenital anomaly of anterior chamber of eye (disorder) [Orphanet:4140]
Anterior chamber anomalies (disorder) [Orphanet:4140]
Congenital anomaly of anterior chamber of eye [Orphanet:4140]
Anterior chamber anomalies [OMIM:Anterior chamber anomalies]
Eye anterior chamber congenital anomaly [Orphanet:4140]
Eye anterior chamber congenital anomaly [MedDRA:10061051]
Congenital anomaly of anterior chamber of eye NOS [MedDRA:10061051]
Multiple and combined congenital anomalies of anterior segment [MedDRA:10061051]
Other congenital anomalies of anterior segment [MedDRA:10061051]
Other specified congenital anomalies of iris and ciliary body [MedDRA:10061051]
Specified congenital anomalies of anterior chamber, chamber angle, and related structures [MedDRA:10061051]
Quality:
Cross references:
Orphanet:4140 "Anterior chamber anomaly" [Orphanet:4140]
OMIM: "Anterior chamber anomalies" [OMIM:Anterior chamber anomalies]
UMLS:C0266546 "Congenital anomaly of anterior chamber of eye" [Orphanet:4140]
Is a (Direct Parents):
HPO         Abnormality of the anterior segment of the globe
MedDRA Congenital anterior segment disorders
Orphanet Abnormality of the eye
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)