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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
agnathia-otocephaly complex  
arthrogryposis multiplex congenita +   
autosomal dominant congenital deafness with onychodystrophy  
autosomal recessive congenital ichthyosis +   
bladder exstrophy-epispadias-cloacal exstrophy complex +   
blepharophimosis +   
caudal regression syndrome  
cleft palate-lateral synechia syndrome  
Compton-North congenital myopathy  
congenital adrenal hyperplasia +   
congenital adrenal insufficiency  
congenital afibrinogenemia +   
congenital amegakaryocytic thrombocytopenia +   
congenital aphakia  
congenital bilateral absence of vas deferens +   
congenital bile acid synthesis defect +   
congenital central hypoventilation syndrome +   
congenital chylothorax  
congenital contractural arachnodactyly  
congenital diaphragmatic hernia +   
congenital diarrhea +   
congenital disorder of glycosylation +   
congenital epulis 
congenital fibrosarcoma  
congenital fibrosis of the extraocular muscles +   
Congenital Foot Deformities +   
Alterations or deviations from normal shape or size which result in a disfigurement of the foot occurring at or before birth.
congenital generalized lipodystrophy +   
congenital granular cell tumor 
congenital heart block +   
congenital heart disease +   
congenital hemolytic anemia +   
congenital hereditary endothelial dystrophy of cornea  
congenital hypogammaglobulinemia 
congenital hypoplastic anemia +   
congenital hypothyroidism +   
congenital hypotrichosis with juvenile macular dystrophy  
congenital intrinsic factor deficiency  
congenital lactase deficiency  
congenital leptin deficiency  
congenital megabladder  
congenital mesoblastic nephroma +   
congenital mirror movement disorder +   
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
congenital myopathy 4A +   
congenital nervous system abnormality +   
congenital nystagmus +   
congenital ptosis +   
congenital stationary night blindness +   
congenital stromal corneal dystrophy  
congenital structural myopathy +   
congenital sucrase-isomaltase deficiency  
congenital syphilis +  
congenital toxoplasmosis  
Corneodermatoosseous Syndrome 
cryptophthalmia +   
Ectrodactyly Cardiopathy Dysmorphism 
Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia 
epidermolysis bullosa with congenital localized absence of skin and deformity of nails  
Familial Streblodactyly 
Foot Deformities, Acquired +   
gastroschisis +   
Hallux Valgus +   
Hallux Varus +  
Hammer Toe Syndrome 
Holt-Oram syndrome +   
hypospadias +   
imperforate anus +   
Kantaputra Gorlin Syndrome 
Keipert syndrome  
Klippel-Feil syndrome +   
Krauss Herman Holmes Syndrome 
large congenital melanocytic nevus  
laryngomalacia +   
Leber congenital amaurosis +   
lethal congenital contracture syndrome +   
lethal congenital glycogen storage disease of heart  
Meckel's diverticulum 
Merlob Grunebaum Reisner Syndrome 
Metatarsal Valgus 
Metatarsus Varus 
MLS syndrome +   
multiple congenital anomalies-hypotonia-seizures syndrome +   
myotonia congenita +   
neural tube defect +   
non-congenital cyst of kidney 
nonsyndromic congenital nail disorder +   
omphalocele  
orofacial cleft +   
Osteofibrous Dysplasia  
palmoplantar keratoderma and congenital alopecia 1  
palmoplantar keratoderma and congenital alopecia 2 
Poland syndrome 
polydactyly +   
popliteal pterygium syndrome +   
primary congenital glaucoma +   
radioulnar synostosis +   
rapidly involuting congenital hemangioma 
severe congenital encephalopathy due to MECP2 mutation  
severe congenital neutropenia +   
Silver-Russell syndrome +   
spondyloepiphyseal dysplasia with congenital joint dislocations  
T-cell immunodeficiency, congenital alopecia, and nail dystrophy  
TORCH syndrome 
visceral heterotaxy +   
Zika virus congenital syndrome 
 acheiropody  
 Acrootoocular Syndrome 
 Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges 
 brachydactyly type E1  
 brachydactyly type E2  
 Brachyphalangy, Polydactyly, and Tibial Aplasia/Hypoplasia  
 CAPOS Syndrome  
 Cleft Palate, Deafness, and Oligodontia 
 Complex Camptosynpolydactyly  
 congenital vertical talus  
 Craniosynostosis, Adelaide Type 
 Daneman Davy Mancer Syndrome 
 Deafness, Congenital Onychodystrophy, Recessive Form 
 distal arthrogryposis type 1 +   
 Distal Symphalangism +   
 Ectrodactyly and Ectodermal Dysplasia without Cleft Lip/Palate 
 ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3  
 Eiken syndrome  
 Fairbank Disease 
 Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome 
 Frias Syndrome 
 Fried Goldberg Mundel Syndrome 
 Frints De Smet Fabry Fryns Syndrome 
 Fuhrmann syndrome  
 Game Friedman Paradice Syndrome 
 Growth Retardation, Small and Puffy Hands and Feet, and Eczema 
 Hairy Palms and Soles 
 hand-foot-genital syndrome  
 Jackson-Weiss syndrome  
 Johnson Munson Syndrome 
 Laurin-Sandrow syndrome  
 Macrodactyly of the Foot 
 Mammary-Digital-Nail Syndrome 
 Metatarsus Varus, Type I 
 Mononen-Karnes-Senac syndrome 
 Monophalangy of Great Toe 
 Nicolaides-Baraitser syndrome  
 oculodentodigital dysplasia +   
 Odontotrichoungual-Digital-Palmar Syndrome 
 Oslam syndrome 
 Partial Aphalangia with Syndactyly and Duplication of Metatarsal IV 
 Pfeiffer Tietze Welte Syndrome 
 Postaxial Polydactyly, with Dental and Vertebral Anomalies 
 preaxial polydactyly II +   
 Radial Defect Robin Sequence 
 Radio-Ulnar Synostosis Type 1 
 Radio-Ulnar Synostosis Type 2 
 Ray Peterson Scott Syndrome 
 Richieri Costa Guion-Almeida Syndrome 
 Sandhaus Ben-Ami Syndrome 
 Second Metatarsal-Metacarpal Syndrome 
 Split Hand, Split Foot, Nystagmus 
 split hand-foot malformation 1 with sensorineural hearing loss  
 Stoll Alembik Dott Syndrome 
 Symphalangism with Multiple Anomalies of Hands and Feet 
 syndromic microphthalmia 8 
 Synpolydactyly 2  
 Synpolydactyly with Foot Anomalies 
 Talipes +   
 Talonavicular Coalition 
 Tarsal Coalition 
 tarsal-carpal coalition syndrome +   
 Teebi hypertelorism syndrome +   
 terminal osseous dysplasia  
 trichorhinophalangeal syndrome type III  
 Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet 
 Ulnar Hypoplasia with Lobster-Claw Deformity of Feet 
 Van Maldergem syndrome +   
 Zechi-Ceide Syndrome 

Synonyms
Exact Synonyms: congenital foot deformity
Primary IDs: MESH:D005532
Definition Sources: MESH:D005532

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