Sclerocornea
Symptom Information:
Symptom ID: | HPO:0000647 | ||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |