Talipes valgus

Symptom Information:

Symptom ID: HPO:0004684
Synonyms:
Talipes valgus (disorder) [Orphanet:21680]
Talipes valgus [Orphanet:21680]
Talipes valgus [OMIM:Talipes valgus]
Talipes-valgus [Orphanet:21680]
Talipes valgus, congenital [Orphanet:21680]
Talipes [MedDRA:10043101]
Club foot congenital [MedDRA:10043101]
Clubfoot [MedDRA:10043101]
Clubfoot (congenital) [MedDRA:10043101]
Congenital clubfoot [MedDRA:10043101]
Congenital metatarsus varus [MedDRA:10043101]
Congenital pes cavus [MedDRA:10043101]
Congenital valgus deformity of foot NOS [MedDRA:10043101]
Congenital varus deformity of foot NOS [MedDRA:10043101]
Fetal talipes [MedDRA:10043101]
Foetal talipes [MedDRA:10043101]
Metatarsus varus, congenital [MedDRA:10043101]
Other congenital valgus deformities of feet [MedDRA:10043101]
Other congenital varus deformities of feet [MedDRA:10043101]
Talipes calcaneovalgus [MedDRA:10043101]
Talipes cavus [MedDRA:10043101]
Talipes equines [MedDRA:10043101]
Talipes equinovarus [MedDRA:10043101]
Talipes equinovarus, congenital [MedDRA:10043101]
Talipes equinus [MedDRA:10043101]
Talipes valgus, congenital [MedDRA:10043101]
Talipes varus, congenital [MedDRA:10043101]
Talipes, unspecified [MedDRA:10043101]
Valgus deformities of feet, congenital [MedDRA:10043101]
Varus deformities of feet, congenital [MedDRA:10043101]
Talipes congenital [MedDRA:10043101]
Congenital valgus foot deformity [MedDRA:10043101]
Pes supinatus [MedDRA:10043101]
Clubfoot (1 patient) [OMIM:Clubfoot (1 patient)]
Clubfoot (in 2 sibs) [OMIM:Clubfoot (in 2 sibs)]
Clubfoot (in some patients) [OMIM:Clubfoot (in some patients)]
Talipes equinovarus (32%) [OMIM:Talipes equinovarus (32%)]
Talipes equinovarus (44%) [OMIM:Talipes equinovarus (44%)]
Talipes equinovarus (clubfoot) [OMIM:Talipes equinovarus (clubfoot)]
Talipes equinovarus (in some patients) [OMIM:Talipes equinovarus (in some patients)]
Talipes equinus [OMIM:Talipes equinus]
Quality:
Cross references:
Orphanet:21680 "Talipes-valgus" [Orphanet:21680]
OMIM: "Talipes valgus" [OMIM:Talipes valgus]
OMIM: "Clubfoot (1 patient)" [OMIM:Clubfoot (1 patient)]
OMIM: "Clubfoot (in 2 sibs)" [OMIM:Clubfoot (in 2 sibs)]
OMIM: "Clubfoot (in some patients)" [OMIM:Clubfoot (in some patients)]
OMIM: "Talipes equinovarus (32%)" [OMIM:Talipes equinovarus (32%)]
OMIM: "Talipes equinovarus (44%)" [OMIM:Talipes equinovarus (44%)]
OMIM: "Talipes equinovarus (clubfoot)" [OMIM:Talipes equinovarus (clubfoot)]
OMIM: "Talipes equinovarus (in some patients)" [OMIM:Talipes equinovarus (in some patients)]
OMIM: "Talipes equinus" [OMIM:Talipes equinus]
UMLS:C0152236 "Talipes valgus" [Orphanet:21680]
Is a (Direct Parents):
HPO         Abnormality of the ankles
Orphanet Abnormality of the ankles
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
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 joint morphology(HPO:0001367)
                Abnormality of lower limb joint(HPO:0100491)
                   Abnormality of the ankles(HPO:0003028)
                      Talipes valgus(HPO:0004684)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of lower limb joint(HPO:0100491)
                         Abnormality of the ankles(HPO:0003028)
                            Talipes valgus(HPO:0004684)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396)
       Musculoskeletal and connective tissue disorders of limbs congenital(MedDRA:10028381)
          Talipes valgus(HPO:0004684)
Database Frequency: 28 / 7739
Resource:

All diseases associated with this symptom:

16p13.11 microdeletion syndrome (Orphanet:261236)
17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
1p36 deletion syndrome (Orphanet:1606)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Barth syndrome (Orphanet:111)
Brachydactyly type C (Orphanet:93384)
CHROMOSOME 2q31.1 DUPLICATION SYNDROME (OMIM:613681)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Catel-Manzke syndrome (Orphanet:1388)
Charcot-Marie-Tooth disease type 4B2 (Orphanet:99956)
Congenital contractural arachnodactyly (Orphanet:115)
Dihydropyrimidinuria (Orphanet:38874)
Distal arthrogryposis type 5D (Orphanet:329457)
Familial clubfoot due to PITX1 point mutation (Orphanet:293150)
Genitopatellar syndrome (Orphanet:85201)
Intellectual deficit - polydactyly - uncombable hair (Orphanet:3082)
Marinesco-Sjögren syndrome (Orphanet:559)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Mesomelic dysplasia, Savarirayan type (Orphanet:85170)
Microphthalmia with limb anomalies (Orphanet:1106)
Moebius syndrome (Orphanet:570)
Pontocerebellar hypoplasia type 8 (Orphanet:324569)
Proteus syndrome (Orphanet:744)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
Schilbach-Rott syndrome (Orphanet:2353)
Schwartz-Jampel syndrome (Orphanet:800)
Stüve-Wiedemann syndrome (Orphanet:3206)
Walker-Warburg syndrome (Orphanet:899)