Talipes calcaneovalgus

Symptom Information:

Symptom ID: HPO:0001884
Synonyms:
Pes calcaneovarus [HPO:0001884]
Pes calcaneovarus [OMIM:Pes calcaneovarus]
Talipes calcaneovalgus [OMIM:Talipes calcaneovalgus]
Quality:
Cross references:
OMIM: "Pes calcaneovarus" [OMIM:Pes calcaneovarus]
OMIM: "Talipes calcaneovalgus" [OMIM:Talipes calcaneovalgus]
Is a (Direct Parents):
HPO         Talipes
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)
                         Positional foot deformity(HPO:0005656)
                            Talipes(HPO:0001883)
                               Talipes calcaneovalgus(HPO:0001884)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 (OMIM:613404)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Carpenter-Waziri syndrome (Orphanet:93973)
Charcot-Marie-Tooth disease type 1E (Orphanet:90658)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Holmes-Gang syndrome (Orphanet:93970)
Juberg-Marsidi syndrome (Orphanet:93972)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B (OMIM:610217)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Smith-Lemli-Opitz syndrome (Orphanet:818)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
[DEL] ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 (OMIM:208085)