Sclerocornea

Symptom Information:

Symptom ID: HPO:0000647
Synonyms:
SCLEROCORNEA [HPO:0000647]
Sclerocornea [OMIM:Sclerocornea]
Sclerocornea [Orphanet:4440]
Sclerocornea (in some patients) [OMIM:Sclerocornea (in some patients)]
Quality:
Cross references:
Orphanet:4440 "Sclerocornea" [Orphanet:4440]
OMIM: "Sclerocornea" [OMIM:Sclerocornea]
OMIM: "Sclerocornea (in some patients)" [OMIM:Sclerocornea (in some patients)]
UMLS:C1853235 "SCLEROCORNEA" [HPO:0000647]
Is a (Direct Parents):
HPO         Corneal opacity
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 cornea(HPO:0000481)
                      Corneal opacity(HPO:0007957)
                         Sclerocornea(HPO:0000647)
MedDRA:
Database Frequency: 25 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
8q21.11 microdeletion syndrome (Orphanet:284160)
Anophthalmia/microphthalmia - esophageal atresia (Orphanet:77298)
BRITTLE CORNEA SYNDROME 2 (OMIM:614170)
CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES (OMIM:269400)
Congenital primary aphakia (Orphanet:83461)
DIGEORGE SYNDROME (OMIM:188400)
Ectodermal dysplasia - blindness (Orphanet:1806)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Isolated congenital sclerocornea (Orphanet:91490)
MICROPHTHALMIA, ISOLATED 3 (OMIM:611038)
MICROPHTHALMIA, SYNDROMIC 14 (OMIM:615877)
MICROPHTHALMIA, SYNDROMIC 7 (OMIM:309801)
Meckel syndrome (Orphanet:564)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Mietens syndrome (Orphanet:2557)
Norrie disease (Orphanet:649)
Oculoauricular syndrome, Schorderet type (Orphanet:157962)
PHACE syndrome (Orphanet:42775)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Van den Ende-Gupta syndrome (Orphanet:2460)
Wolf-Hirschhorn syndrome (Orphanet:280)
Yunis-Varon syndrome (Orphanet:3472)