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784010006: Otopalatodigital syndrome spectrum disorder (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3761048015 Otopalatodigital syndrome spectrum disorder en Synonym Active Entire term case insensitive SNOMED CT core module
3761049011 OPD (otopalatodigital) spectrum disorder en Synonym Active Entire term case sensitive SNOMED CT core module
3761050011 Otopalatodigital syndrome spectrum disorder (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

5 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Otopalatodigital syndrome spectrum disorder Is a Congenital skeletal dysplasia true Inferred relationship Existential restriction modifier
Otopalatodigital syndrome spectrum disorder Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Otopalatodigital syndrome spectrum disorder Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Otopalatodigital syndrome spectrum disorder Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Otopalatodigital syndrome spectrum disorder Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Otopalatodigital syndrome spectrum disorder Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Otopalatodigital syndrome spectrum disorder Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier
Otopalatodigital syndrome spectrum disorder Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
Otopalatodigital syndrome spectrum disorder Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Otopalatodigital syndrome spectrum disorder Is a X-linked dominant hereditary disease true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Frontometaphyseal dysplasia Is a True Otopalatodigital syndrome spectrum disorder Inferred relationship Existential restriction modifier
Terminal osseous dysplasia and pigmentary defect syndrome Is a True Otopalatodigital syndrome spectrum disorder Inferred relationship Existential restriction modifier
Oto-palato-digital syndrome, type I Is a True Otopalatodigital syndrome spectrum disorder Inferred relationship Existential restriction modifier
Oto-palato-digital syndrome, type II Is a True Otopalatodigital syndrome spectrum disorder Inferred relationship Existential restriction modifier
Melnick-Needles syndrome Is a True Otopalatodigital syndrome spectrum disorder Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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