Talipes cavus equinovarus
Symptom Information:
Symptom ID: | HPO:0004696 | |||||||||||||||||||||||||||||||||||||||||||||||
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 the foot(HPO:0001760) Positional foot deformity(HPO:0005656) Talipes(HPO:0001883) Talipes equinovarus(HPO:0001762) Talipes cavus equinovarus(HPO:0004696) 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 cavus equinovarus(HPO:0004696) |
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Database Frequency: | 13 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |
48,XXYY syndrome | (Orphanet:10) |
Autosomal dominant dopa-responsive dystonia | (Orphanet:98808) |
Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
Barth syndrome | (Orphanet:111) |
CHROMOSOME 2q31.1 DUPLICATION SYNDROME | (OMIM:613681) |
Charcot-Marie-Tooth disease type 4B2 | (Orphanet:99956) |
Charcot-Marie-Tooth disease type 4D | (Orphanet:99950) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Dihydropyrimidinuria | (Orphanet:38874) |
Distal arthrogryposis type 5D | (Orphanet:329457) |
Familial clubfoot due to PITX1 point mutation | (Orphanet:293150) |
Moebius syndrome | (Orphanet:570) |