Popliteal pterygium
Symptom Information:
Symptom ID: | HPO:0009756 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
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) Popliteal pterygium(HPO:0009756) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal joint morphology(HPO:0001367) Pterygium(HPO:0001059) Popliteal pterygium(HPO:0009756) MedDRA: |
||||
Database Frequency: | 9 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant popliteal pterygium syndrome | (Orphanet:1300) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Autosomal recessive omodysplasia | (Orphanet:93329) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
Bartsocas-Papas syndrome | (Orphanet:1234) |
Embryonary disorganization syndrome | (Orphanet:1664) |
Lethal multiple pterygium syndrome | (Orphanet:33108) |
Oto-onycho-peroneal syndrome | (Orphanet:2793) |
Tibial aplasia - ectrodactyly | (Orphanet:3329) |