Talipes valgus
Symptom Information:
Symptom ID: | HPO:0004684 | |||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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 lower limb joint(HPO:0100491) Abnormality of the ankles(HPO:0003028) Talipes valgus(HPO:0004684) Abnormal joint morphology(HPO:0001367) 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) |
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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) |