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763213001: Conductive deafness, ptosis, skeletal anomalies syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3638186014 Jackson Barr syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3638187017 Conductive deafness, ptosis, skeletal anomalies syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3638188010 Conductive deafness, ptosis, skeletal anomalies syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Conductive deafness, ptosis, skeletal anomalies syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Conductive deafness, ptosis, skeletal anomalies syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Conductive deafness, ptosis, skeletal anomalies syndrome Is a Skin lesion true Inferred relationship Existential restriction modifier
Conductive deafness, ptosis, skeletal anomalies syndrome Is a Ectodermal dysplasia with hair-tooth defects true Inferred relationship Existential restriction modifier
Conductive deafness, ptosis, skeletal anomalies syndrome Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Conductive deafness, ptosis, skeletal anomalies syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Conductive deafness, ptosis, skeletal anomalies syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Conductive deafness, ptosis, skeletal anomalies syndrome Finding site Ectoderm structure true Inferred relationship Existential restriction modifier 2
Conductive deafness, ptosis, skeletal anomalies syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Conductive deafness, ptosis, skeletal anomalies syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Conductive deafness, ptosis, skeletal anomalies syndrome Finding site Ectoderm structure false Inferred relationship Existential restriction modifier 1
Conductive deafness, ptosis, skeletal anomalies syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Conductive deafness, ptosis, skeletal anomalies syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Conductive deafness, ptosis, skeletal anomalies syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Conductive deafness, ptosis, skeletal anomalies syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Conductive deafness, ptosis, skeletal anomalies syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Conductive deafness, ptosis, skeletal anomalies syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 2
Conductive deafness, ptosis, skeletal anomalies syndrome Finding site Hair structure true Inferred relationship Existential restriction modifier 3
Conductive deafness, ptosis, skeletal anomalies syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 4
Conductive deafness, ptosis, skeletal anomalies syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Conductive deafness, ptosis, skeletal anomalies syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Conductive deafness, ptosis, skeletal anomalies syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Conductive deafness, ptosis, skeletal anomalies syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Conductive deafness, ptosis, skeletal anomalies syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Conductive deafness, ptosis, skeletal anomalies syndrome Finding site Tooth structure false Inferred relationship Existential restriction modifier 4
Conductive deafness, ptosis, skeletal anomalies syndrome Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier
Conductive deafness, ptosis, skeletal anomalies syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Conductive deafness, ptosis, skeletal anomalies syndrome Is a Hereditary disorder of tooth true Inferred relationship Existential restriction modifier
Conductive deafness, ptosis, skeletal anomalies syndrome Is a Oral lesion true Inferred relationship Existential restriction modifier
Conductive deafness, ptosis, skeletal anomalies syndrome Is a Malformation of teeth true Inferred relationship Existential restriction modifier
Conductive deafness, ptosis, skeletal anomalies syndrome Finding site Structure of dentition true Inferred relationship Existential restriction modifier 4
Conductive deafness, ptosis, skeletal anomalies syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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