Abnormality of the tarsal bones
Symptom Information:
Symptom ID: | HPO:0001850 | ||||
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) MedDRA: |
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Database Frequency: | 40 / 7739 | ||||
Resource: |
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) |