OMOP Concept 606884
Hereditary disorder of tooth
StandardConditionSNOMED1148766007Disorder
Maps from
13
Descendants
109
Valid from
31 Jul 2021
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
13 source codes normalize to Hereditary disorder of tooth via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Hereditary disorder of tooth across source vocabularies.
- enfermedad dental hereditaria
- Hereditary disorder of tooth (disorder)
- trastorno dental hereditario
- trastorno hereditario de diente
- trastorno hereditario de diente (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(22)Roll up to these when you need a wider cohort.
- 1Digestive system hereditary disorder
- 1Tooth disorder
- 2Disorder of digestive organ
- 2Disorder of digestive system
- 2Disorder of teeth AND/OR supporting structures
- 2Hereditary disorder by system
- 2Tooth finding
- 3Digestive system finding
- 3Disease of mouth
- 3Disorder of body system
- 3Disorder of jaw
- 3Disorder of upper digestive tract
- 3Hereditary disease
- 3Oral cavity finding
- 4Clinical finding
- 4Disease
- 4Disorder of digestive tract
- 4Disorder of head
- 4Finding of head region
- 4Finding of mouth region
- 4Genetic disease
- 5Head finding
Narrower concepts
(109)Included automatically when you query with descendants.
- 14H leukodystrophy
- 1Ackerman syndrome
- 1ADULT (acro-dermato-ungual-lacrimal-tooth) syndrome
- 1Amelogenesis imperfecta
- 1Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA gain of function mutation
- 1Anhidrotic ectodermal dysplasia with immune deficiency due to IKBKB GOF mutation
- 1Anterior maxillary protrusion, strabismus, intellectual disability syndrome
- 1Arthrogryposis and ectodermal dysplasia syndrome
- 1Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
- 1Autosomal recessive hypohidrotic ectodermal dysplasia syndrome
- 1Book syndrome
- 1Cerebellar-facial-dental syndrome
- 1Cleidocranial dysostosis
- 1Conductive deafness, ptosis, skeletal anomalies syndrome
- 1Congenital deafness with labyrinthine aplasia, microtia and microdontia
- 1Contracture with ectodermal dysplasia and orofacial cleft syndrome
- 1Craniosynostosis and dental anomalies syndrome
- 1Curly hair, acral keratoderma, caries syndrome
- 1Curry-Hall syndrome
- 1Deafness, enamel hypoplasia, nail defect syndrome
- 1Dentin dysplasia
- 1Dentinogenesis imperfecta
- 1Dermatoosteolysis Kirghizian type
- 1Dermo-odonto dysplasia
- 1Developmental absence of tooth
Showing 25 of 109. Retrieve the full set via the API.
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