Hereditary disorder of tooth

Code	`1148766007`
Semantic tag	disorder
Module	international
Definition	defined
Effective time	20210731

12089330004H leucodystrophy disorder

720464003ADULT (acro-dermato-ungual-lacrimal-tooth) syndrome disorder

722280000Ackerman syndrome disorder

78494001Amelogenesis imperfecta disorder

1354646005Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA gain of function mutation disorder

1366698006Anhidrotic ectodermal dysplasia with immune deficiency due to IKBKB GOF mutation disorder

1222706005Anterior maxillary protrusion, strabismus, intellectual disability syndrome disorder

786039009Arthrogryposis and ectodermal dysplasia syndrome disorder

7731005Autosomal dominant hypohidrotic ectodermal dysplasia syndrome disorder

27025001Autosomal recessive hypohidrotic ectodermal dysplasia syndrome disorder

722296002Book syndrome disorder

1237475006Cerebellar-facial-dental syndrome disorder

65976001Cleidocranial dysostosis disorder

763213001Conductive deafness, ptosis, skeletal anomalies syndrome disorder

702360007Congenital deafness with labyrinthine aplasia, microtia and microdontia disorder

720746006Contracture with ectodermal dysplasia and orofacial cleft syndrome disorder

773332008Craniosynostosis and dental anomalies syndrome disorder

763686007Curly hair, acral keratoderma, caries syndrome disorder

277807007Curry-Hall syndrome disorder

721085000Deafness, enamel hypoplasia, nail defect syndrome disorder

109492001Dentin dysplasia disorder

196286005Dentinogenesis imperfecta disorder

721090002Dermatoosteolysis Kirghizian type disorder

721091003Dermo-odonto dysplasia disorder

234951001Developmental absence of tooth disorder

771335004Ectodermal dysplasia syndactyly syndrome disorder

734018003Ectodermal dysplasia trichoodontoonychial type disorder

721208007Ectodermal dysplasia with blindness syndrome disorder

1179293006Erythrokeratodermia cardiomyopathy syndrome disorder

721843003GAPO syndrome disorder

719973009Haim Munk syndrome disorder

773553003Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome disorder

239007005Hypohidrotic X-linked ectodermal dysplasia disorder

763658004Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome disorder

367520004Incontinentia pigmenti syndrome disorder

764995008Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome disorder

445257004Nance-Horan syndrome disorder

723442008Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome disorder

1255268002Oculocerebrodental syndrome disorder

722061006Oculoosteocutaneous syndrome disorder

722062004Oculotrichodysplasia disorder

722063009Odonto-tricho-ungual-digito-palmar syndrome disorder

239028001Odontotrichomelic syndrome disorder

1237343009Otodental syndrome disorder

771240009Pilodental dysplasia, refractive errors syndrome disorder

773279006Postaxial polydactyly, dental, vertebral anomalies syndrome disorder

1231153007Primary failure of tooth eruption disorder

18899000Schinzel-Giedion syndrome disorder

716092007Schmitt Gillenwater Kelly syndrome disorder

700062000Schöpf-Schulz-Passarge syndrome disorder

719306007Steatocystoma multiplex with natal tooth syndrome disorder

723584003Stern Lubinsky Durrie syndrome disorder

723583009Steroid dehydrogenase deficiency and dental anomaly syndrome disorder

771265006Teebi Shaltout syndrome disorder

777998000Temtamy preaxial brachydactyly syndrome disorder

766813000Trichoodontoonychial dysplasia disorder

719910004Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome disorder

7037003XTE syndrome disorder

Parents (2)

Children (58)