Abnormality of the tarsal bones

Symptom Information:

Symptom ID: HPO:0001850
Tarsal anomaly [Orphanet:21280]
Tarsal anomaly/fusion/synostosis [Orphanet:21280]
Cross references:
HPO:0008363 "Aplasia/Hypoplasia of the tarsal bones" [Orphanet:21280]
Orphanet:21280 "Tarsal anomaly/fusion/synostosis" [Orphanet:21280]
Is a (Direct Parents):
Orphanet Abnormality of the lower limb
HPO         Abnormality of the foot
Is a (Whole tree): HPO:
    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)
Database Frequency: 40 / 7739

All diseases associated with this symptom:

Acromesomelic dysplasia, Grebe type (Orphanet:2098)
Acromesomelic dysplasia, Hunter-Thomson type (Orphanet:968)
Acropectorovertebral dysplasia (Orphanet:957)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Carpotarsal osteochondromatosis (Orphanet:2767)
Cleft palate - stapes fixation - oligodontia (Orphanet:2010)
Dermatoosteolysis, Kirghizian type (Orphanet:1657)
Distal limb deficiencies - micrognathia syndrome (Orphanet:1307)
Dysplasia epiphysealis hemimelica (Orphanet:1822)
Fibular aplasia - complex brachydactyly (Orphanet:2639)
Fuhrmann syndrome (Orphanet:2854)
Fukuda-Miyanomae-Nakata syndrome (Orphanet:2060)
Hand-foot-genital syndrome (Orphanet:2438)
Humero-radial synostosis (Orphanet:3265)
Jackson-Weiss syndrome (Orphanet:1540)
Laurin-Sandrow syndrome (Orphanet:2378)
Lethal Larsen-like syndrome (Orphanet:2371)
Limb transversal defect - cardiac anomaly (Orphanet:2492)
McKusick-Kaufman syndrome (Orphanet:2473)
Menkes disease (Orphanet:565)
Mesomelia-synostoses syndrome (Orphanet:2496)
Mesomelic dwarfism, Nievergelt type (Orphanet:2633)
Mesomelic dysplasia, Kantaputra type (Orphanet:1836)
Microphthalmia with limb anomalies (Orphanet:1106)
Mononen-Karnes-Senac syndrome (Orphanet:2565)
Monosomy 9p (Orphanet:261112)
Muenke syndrome (Orphanet:53271)
Multiple epiphyseal dysplasia (Orphanet:251)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 10 (Orphanet:2756)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Otopalatodigital syndrome type 2 (Orphanet:90652)
Posterior fusion of lumbosacral vertebrae - blepharoptosis (Orphanet:2064)
Proximal symphalangism (Orphanet:3250)
Schneckenbecken dysplasia (Orphanet:3144)
Sheldon-Hall syndrome (Orphanet:1147)
Symphalangism with multiple anomalies of hands and feet (Orphanet:3246)
Tarsal-carpal coalition syndrome (Orphanet:1412)
Torg-Winchester syndrome (Orphanet:3460)
Verloove Vanhorick-Brubakk syndrome (Orphanet:3429)