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733069009: Deafness, vitiligo, achalasia syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3498670013 Deafness, vitiligo, achalasia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3498671012 Deafness, vitiligo, achalasia 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
Deafness, vitiligo, achalasia syndrome Is a Congenital deficiency of pigment of skin true Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Is a Vitiligo true Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Is a Congenital deafness true Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Is a Hearing loss associated with syndrome true Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Is a Short stature disorder true Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Is a Congenital achalasia of esophagus true Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Is a Genetic disorder of skin pigmentation true Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Deafness, vitiligo, achalasia syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Deafness, vitiligo, achalasia syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 3
Deafness, vitiligo, achalasia syndrome Finding site Cardioesophageal junction structure false Inferred relationship Existential restriction modifier 5
Deafness, vitiligo, achalasia syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 6
Deafness, vitiligo, achalasia syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 7
Deafness, vitiligo, achalasia syndrome Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 6
Deafness, vitiligo, achalasia syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 6
Deafness, vitiligo, achalasia syndrome Finding site Esophageal structure false Inferred relationship Existential restriction modifier 4
Deafness, vitiligo, achalasia syndrome Has interpretation Abnormal true Inferred relationship Existential restriction modifier 4
Deafness, vitiligo, achalasia syndrome Interprets Motility true Inferred relationship Existential restriction modifier 4
Deafness, vitiligo, achalasia syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 7
Deafness, vitiligo, achalasia syndrome Finding site Inner ear structure false Inferred relationship Existential restriction modifier 7
Deafness, vitiligo, achalasia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Deafness, vitiligo, achalasia syndrome Finding site Inner ear structure true Inferred relationship Existential restriction modifier 2
Deafness, vitiligo, achalasia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Deafness, vitiligo, achalasia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Deafness, vitiligo, achalasia syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Deafness, vitiligo, achalasia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Deafness, vitiligo, achalasia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Deafness, vitiligo, achalasia syndrome Finding site Cardioesophageal junction structure true Inferred relationship Existential restriction modifier 1
Deafness, vitiligo, achalasia syndrome Associated morphology Hypopigmentation true Inferred relationship Existential restriction modifier 3
Deafness, vitiligo, achalasia syndrome Is a Congenital anomaly of ear with impairment of hearing true Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Is a Congenital anomaly of inner ear true Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 5
Deafness, vitiligo, achalasia syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Deafness, vitiligo, achalasia syndrome Interprets Height / growth measure true Inferred relationship Existential restriction modifier 6
Deafness, vitiligo, achalasia syndrome Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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