Pterygium
Symptom Information:
Symptom ID: | HPO:0001059 | |||||||||||||||
Synonyms: |
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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 integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Regional abnormality of skin(HPO:0011356) Pterygium(HPO:0001059) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal joint morphology(HPO:0001367) Pterygium(HPO:0001059) MedDRA: Eye disorders(MedDRA:10015919) Anterior eye structural change, deposit and degeneration(MedDRA:10002693) Conjunctival structural change, deposit and degeneration(MedDRA:10010735) Pterygium(HPO:0001059) |
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Database Frequency: | 16 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
Arthrogryposis multiplex congenita | (Orphanet:1037) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Autosomal recessive omodysplasia | (Orphanet:93329) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
BRUCK SYNDROME 1 | (OMIM:259450) |
BRUCK SYNDROME 2 | (OMIM:609220) |
Bruck syndrome | (Orphanet:2771) |
Fetal akinesia deformation sequence | (Orphanet:994) |
Junctional epidermolysis bullosa - pyloric atresia | (Orphanet:79403) |
Kyphomelic dysplasia | (Orphanet:1801) |
Lichen planopilaris | (Orphanet:525) |
Neu-Laxova syndrome | (Orphanet:2671) |
PHAVER syndrome | (Orphanet:2876) |
Pterygium of the conjunctiva, familial form | (Orphanet:2989) |
Short stature - craniofacial anomalies - genital hypoplasia | (Orphanet:2994) |
Xeroderma pigmentosum | (Orphanet:910) |