Calcaneovalgus deformity

Symptom Information:

Symptom ID: HPO:0001848
Synonyms:
Calcaneovalgus [HPO:0001848]
Calcaneovalgus Foot [HPO:0001848]
Valgus position of the calcaneus [HPO:0001848]
Calcaneovalgus [OMIM:Calcaneovalgus]
Valgus position of the calcaneus [OMIM:Valgus position of the calcaneus]
Calcaneovalgus deformities [OMIM:Calcaneovalgus deformities]
Calcaneovalgus deformity (in some patients) [OMIM:Calcaneovalgus deformity (in some patients)]
Quality:
Cross references:
OMIM: "Calcaneovalgus" [OMIM:Calcaneovalgus]
OMIM: "Valgus position of the calcaneus" [OMIM:Valgus position of the calcaneus]
OMIM: "Calcaneovalgus deformities" [OMIM:Calcaneovalgus deformities]
OMIM: "Calcaneovalgus deformity (in some patients)" [OMIM:Calcaneovalgus deformity (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of the calcaneus
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:
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)