Pterygium

Symptom Information:

Symptom ID: HPO:0001059
Synonyms:
Pterygia [HPO:0001059]
Pterygium (disorder) [Orphanet:4540]
Pterygium [Orphanet:4540]
Pterygia [OMIM:Pterygia]
Pterygium [OMIM:Pterygium]
Pterygion [Orphanet:4540]
Pterygium [MedDRA:10037263]
Central pterygium [MedDRA:10037263]
Double pterygium [MedDRA:10037263]
Peripheral pterygium, progressive [MedDRA:10037263]
Peripheral pterygium, stationary [MedDRA:10037263]
Pterygium, unspecified [MedDRA:10037263]
Recurrent pterygium [MedDRA:10037263]
Pterygia (knees and elbows) [OMIM:Pterygia (knees and elbows)]
Pterygium (elbows and knees) [OMIM:Pterygium (elbows and knees)]
Quality:
Cross references:
Orphanet:4540 "Pterygion" [Orphanet:4540]
OMIM: "Pterygia" [OMIM:Pterygia]
OMIM: "Pterygium" [OMIM:Pterygium]
OMIM: "Pterygia (knees and elbows)" [OMIM:Pterygia (knees and elbows)]
OMIM: "Pterygium (elbows and knees)" [OMIM:Pterygium (elbows and knees)]
UMLS:C0033999 "Pterygium" [HPO:0001059]
UMLS:C0033999 "Pterygium" [Orphanet:4540]
Is a (Direct Parents):
MedDRA Conjunctival structural change, deposit and degeneration
HPO         Regional abnormality of skin
Orphanet Abnormality of the eye
HPO         Abnormal joint morphology
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)
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)