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1187212004: Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Nov 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4672737014 Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4672738016 Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Is a Developmental delay true Inferred relationship Existential restriction modifier
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Is a Poor muscle tone true Inferred relationship Existential restriction modifier
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Is a Congenital septal defect of heart true Inferred relationship Existential restriction modifier
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Is a Congenital anomaly of skeletal muscle true Inferred relationship Existential restriction modifier
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Is a Congenital strabismus true Inferred relationship Existential restriction modifier
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Interprets Muscle tone true Inferred relationship Existential restriction modifier 4
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Finding site Eye region structure true Inferred relationship Existential restriction modifier 2
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Finding site Cardiac septum structure true Inferred relationship Existential restriction modifier 3
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Associated morphology Defect true Inferred relationship Existential restriction modifier 3
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Is a Decreased muscle tone true Inferred relationship Existential restriction modifier
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome Has interpretation Decreased 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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