Posterior embryotoxon

Symptom Information:

Symptom ID: HPO:0000627
Synonyms:
Embryotoxon [HPO:0000627]
Embryotoxon [Orphanet:4460]
Arcus senilis (disorder) [Orphanet:4460]
Embryotoxon (disorder) [Orphanet:4460]
Posterior embryotoxon [OMIM:Posterior embryotoxon]
Quality:
Cross references:
HPO:0001084 "Corneal arcus" [Orphanet:4460]
Orphanet:4460 "Embryotoxon" [Orphanet:4460]
OMIM: "Posterior embryotoxon" [OMIM:Posterior embryotoxon]
UMLS:C0344531 "Embryotoxon" [Orphanet:4460]
Is a (Direct Parents):
Orphanet Abnormality of the eye
HPO         Abnormality of the line of Schwalbe
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 cornea(HPO:0000481)
                      Abnormality of the line of Schwalbe(HPO:0008048)
                         Posterior embryotoxon(HPO:0000627)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
AXENFELD-RIEGER SYNDROME, TYPE 3 (OMIM:602482)
Alagille syndrome due to 20p12 microdeletion (Orphanet:261600)
Alagille syndrome due to a JAG1 point mutation (Orphanet:261619)
Axenfeld-Rieger syndrome (Orphanet:782)
DIGEORGE SYNDROME (OMIM:188400)
Dandy-Walker malformation - postaxial polydactyly (Orphanet:1566)
Distal monosomy 6p (Orphanet:96125)
FOVEAL HYPOPLASIA 2 (OMIM:609218)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
SHORT syndrome (Orphanet:3163)
Uveal coloboma - cleft lip and palate - intellectual deficit (Orphanet:1473)
VELOCARDIOFACIAL SYNDROME (OMIM:192430)
Williams syndrome (Orphanet:904)
Zellweger syndrome (Orphanet:912)