Metatarsus adductus

Symptom Information:

Symptom ID: HPO:0001840
Synonyms:
Forefoot varus [HPO:0001840]
Intoe [HPO:0001840]
Metatarsus adductovarsus [HPO:0001840]
Metatarsus varus [HPO:0001840]
Metatarsus varus [Orphanet:21640]
Metatarsus adductus (disorder) [Orphanet:22560]
Metatarsus varus (disorder) [Orphanet:21640]
Metatarsus adductus (disorder) [Orphanet:21640]
Metatarsus adductus [Orphanet:22560]
Metatarsus adductus [Orphanet:21640]
Congenital metatarsus varus [Orphanet:21640]
Metatarsus adductus [OMIM:Metatarsus adductus]
Metatarsus varus [OMIM:Metatarsus varus]
Talipes-varus/metatarsal varus [Orphanet:21640]
Metatarsus varus, congenital [Orphanet:21640]
Talipes [MedDRA:10043101]
Club foot congenital [MedDRA:10043101]
Clubfoot [MedDRA:10043101]
Clubfoot (congenital) [MedDRA:10043101]
Congenital clubfoot [MedDRA:10043101]
Congenital metatarsus varus [MedDRA:10043101]
Congenital pes cavus [MedDRA:10043101]
Congenital valgus deformity of foot NOS [MedDRA:10043101]
Congenital varus deformity of foot NOS [MedDRA:10043101]
Fetal talipes [MedDRA:10043101]
Foetal talipes [MedDRA:10043101]
Metatarsus varus, congenital [MedDRA:10043101]
Other congenital valgus deformities of feet [MedDRA:10043101]
Other congenital varus deformities of feet [MedDRA:10043101]
Talipes calcaneovalgus [MedDRA:10043101]
Talipes cavus [MedDRA:10043101]
Talipes equines [MedDRA:10043101]
Talipes equinovarus [MedDRA:10043101]
Talipes equinovarus, congenital [MedDRA:10043101]
Talipes equinus [MedDRA:10043101]
Talipes valgus, congenital [MedDRA:10043101]
Talipes varus, congenital [MedDRA:10043101]
Talipes, unspecified [MedDRA:10043101]
Valgus deformities of feet, congenital [MedDRA:10043101]
Varus deformities of feet, congenital [MedDRA:10043101]
Talipes congenital [MedDRA:10043101]
Congenital valgus foot deformity [MedDRA:10043101]
Pes supinatus [MedDRA:10043101]
Clubfoot (1 patient) [OMIM:Clubfoot (1 patient)]
Clubfoot (in 2 sibs) [OMIM:Clubfoot (in 2 sibs)]
Clubfoot (in some patients) [OMIM:Clubfoot (in some patients)]
Talipes equinovarus (32%) [OMIM:Talipes equinovarus (32%)]
Talipes equinovarus (44%) [OMIM:Talipes equinovarus (44%)]
Talipes equinovarus (clubfoot) [OMIM:Talipes equinovarus (clubfoot)]
Talipes equinovarus (in some patients) [OMIM:Talipes equinovarus (in some patients)]
Talipes equinus [OMIM:Talipes equinus]
Quality:
Cross references:
Orphanet:22560 "Metatarsus adductus" [Orphanet:22560]
Orphanet:21640 "Talipes-varus/metatarsal varus" [Orphanet:21640]
OMIM: "Metatarsus adductus" [OMIM:Metatarsus adductus]
OMIM: "Metatarsus varus" [OMIM:Metatarsus varus]
OMIM: "Clubfoot (1 patient)" [OMIM:Clubfoot (1 patient)]
OMIM: "Clubfoot (in 2 sibs)" [OMIM:Clubfoot (in 2 sibs)]
OMIM: "Clubfoot (in some patients)" [OMIM:Clubfoot (in some patients)]
OMIM: "Talipes equinovarus (32%)" [OMIM:Talipes equinovarus (32%)]
OMIM: "Talipes equinovarus (44%)" [OMIM:Talipes equinovarus (44%)]
OMIM: "Talipes equinovarus (clubfoot)" [OMIM:Talipes equinovarus (clubfoot)]
OMIM: "Talipes equinovarus (in some patients)" [OMIM:Talipes equinovarus (in some patients)]
OMIM: "Talipes equinus" [OMIM:Talipes equinus]
UMLS:C0265648 "Metatarsus adductus" [Orphanet:22560]
UMLS:C0265648 "Metatarsus adductus" [Orphanet:21640]
UMLS:C0265647 "Congenital metatarsus varus" [Orphanet:21640]
Is a (Direct Parents):
Orphanet Talipes equinovarus
HPO         Abnormality of the metatarsal bones
Orphanet Abnormality of the hallux
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
Orphanet Abnormality of the ankles
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)
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)