Anterior segment dysgenesis

Symptom Information:

Symptom ID: HPO:0007700
Synonyms:
Anterior chamber cleavage defect [HPO:0007700]
Anterior chamber cleavage disorder [HPO:0007700]
Anterior chamber malformation [HPO:0007700]
Anterior chamber mesodermal anomalies [HPO:0007700]
Anterior segment mesencyhmal dysgenesis [HPO:0007700]
Anterior segment ocular dysgenesis [HPO:0007700]
Anterior chamber cleavage defect [OMIM:Anterior chamber cleavage defect]
Anterior chamber cleavage disorder [OMIM:Anterior chamber cleavage disorder]
Anterior chamber mesodermal anomalies [OMIM:Anterior chamber mesodermal anomalies]
Anterior segment ocular dysgenesis [OMIM:Anterior segment ocular dysgenesis]
Anterior chamber malformation (WWS) [OMIM:Anterior chamber malformation (WWS)]
Quality:
Cross references:
OMIM: "Anterior chamber cleavage defect" [OMIM:Anterior chamber cleavage defect]
OMIM: "Anterior chamber cleavage disorder" [OMIM:Anterior chamber cleavage disorder]
OMIM: "Anterior chamber mesodermal anomalies" [OMIM:Anterior chamber mesodermal anomalies]
OMIM: "Anterior segment ocular dysgenesis" [OMIM:Anterior segment ocular dysgenesis]
OMIM: "Anterior chamber malformation (WWS)" [OMIM:Anterior chamber malformation (WWS)]
Is a (Direct Parents):
HPO         Abnormality of the anterior chamber
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)
                      Anterior segment dysgenesis(HPO:0007700)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM,AND TRACHEAL STENOSIS (OMIM:601427)
CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES (OMIM:269400)
Familial ocular anterior segment mesenchymal dysgenesis (Orphanet:88632)
Isolated ectopia lentis (Orphanet:1885)
LAMBOTTE SYNDROME (OMIM:245552)
MARFANOID HYPERMOBILITY SYNDROME (OMIM:154750)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 (OMIM:236670)
Peters-plus syndrome (Orphanet:709)
SHORT syndrome (Orphanet:3163)