Calcaneovalgus deformity
Symptom Information:
Symptom ID: | HPO:0001848 | |||||||
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 skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the lower limb(HPO:0002814) Abnormality of the foot(HPO:0001760) Abnormality of the tarsal bones(HPO:0001850) Abnormality of the calcaneus(HPO:0008364) Calcaneovalgus deformity(HPO:0001848) MedDRA: |
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Database Frequency: | 12 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
ARTHROGRYPOSIS, DISTAL, TYPE 1A | (OMIM:108120) |
Arthrogryposis with oculomotor limitation and electroretinal anomalies | (Orphanet:1154) |
Congenital vertical talus | (Orphanet:178382) |
Digitotalar dysmorphism | (Orphanet:1146) |
Distal arthrogryposis type 5D | (Orphanet:329457) |
Ehlers-Danlos syndrome, cardiac valvular type | (Orphanet:230851) |
Gordon syndrome | (Orphanet:376) |
NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX | (OMIM:162370) |
Neu-Laxova syndrome | (Orphanet:2671) |
Sheldon-Hall syndrome | (Orphanet:1147) |
Weaver syndrome | (Orphanet:3447) |