Metatarsus adductus
Symptom Information:
Symptom ID: | HPO:0001840 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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 metatarsal bones(HPO:0001832) Metatarsus adductus(HPO:0001840) 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) Metatarsus adductus(HPO:0001840) |
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Database Frequency: | 49 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |
1p36 deletion syndrome | (Orphanet:1606) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
48,XXYY syndrome | (Orphanet:10) |
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 | (OMIM:170995) |
Acrocraniofacial dysostosis | (Orphanet:949) |
Arthrogryposis with oculomotor limitation and electroretinal anomalies | (Orphanet:1154) |
Autosomal recessive facio-digito-genital syndrome | (Orphanet:1974) |
BRACHMANN-DE LANGE-LIKE FACIAL CHANGES WITH MICROCEPHALY, METATARSUSADDUCTUS, AND DEVELOPMENTAL DELAY | (OMIM:112370) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
Barth syndrome | (Orphanet:111) |
CARPENTER SYNDROME 1 | (OMIM:201000) |
CHROMOSOME 2q31.1 DUPLICATION SYNDROME | (OMIM:613681) |
CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS | (OMIM:608279) |
Carpenter syndrome | (Orphanet:65759) |
Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
Charcot-Marie-Tooth disease type 4B2 | (Orphanet:99956) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Dihydropyrimidinuria | (Orphanet:38874) |
Distal arthrogryposis type 5D | (Orphanet:329457) |
Dubowitz syndrome | (Orphanet:235) |
Familial clubfoot due to PITX1 point mutation | (Orphanet:293150) |
Frank-Ter Haar syndrome | (Orphanet:137834) |
Gordon syndrome | (Orphanet:376) |
HUNTER-MACDONALD SYNDROME | (OMIM:611962) |
Hurler syndrome | (Orphanet:93473) |
Intellectual deficit - cataracts - calcified pinnae - myopathy | (Orphanet:3042) |
Larsen-like syndrome, B3GAT3 type | (Orphanet:284139) |
METATARSUS VARUS, TYPE I | (OMIM:156520) |
Moebius syndrome | (Orphanet:570) |
Monosomy 5p | (Orphanet:281) |
Mucopolysaccharidosis type 7 | (Orphanet:584) |
Multiple epiphyseal dysplasia, Lowry type | (Orphanet:166016) |
Oculocerebrofacial syndrome, Kaufman type | (Orphanet:2707) |
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) | (OMIM:214100) |
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) | (OMIM:214110) |
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) | (OMIM:614866) |
SANTOS SYNDROME | (OMIM:613005) |
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY | (OMIM:181405) |
Sheldon-Hall syndrome | (Orphanet:1147) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification | (Orphanet:93358) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Trismus - pseudocamptodactyly | (Orphanet:3377) |
W syndrome | (Orphanet:2804) |
Weaver syndrome | (Orphanet:3447) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
Zellweger syndrome | (Orphanet:912) |