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239024004: Ectodermal dysplasia, syndactyly and pili torti (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
358203015 Ectodermal dysplasia, syndactyly and pili torti en Synonym Active Case insensitive SNOMED CT core
627984013 Ectodermal dysplasia, syndactyly and pili torti (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ectodermal dysplasia, syndactyly and pili torti Pathological process Pathological developmental process true Inferred relationship Some 2
Ectodermal dysplasia, syndactyly and pili torti Occurrence Congenital true Inferred relationship Some 1
Ectodermal dysplasia, syndactyly and pili torti Pathological process Pathological developmental process true Inferred relationship Some 1
Ectodermal dysplasia, syndactyly and pili torti Finding site Ectoderm structure true Inferred relationship Some 1
Ectodermal dysplasia, syndactyly and pili torti Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Ectodermal dysplasia, syndactyly and pili torti Occurrence Congenital true Inferred relationship Some 4
Ectodermal dysplasia, syndactyly and pili torti Finding site Hair structure true Inferred relationship Some 4
Ectodermal dysplasia, syndactyly and pili torti Associated morphology Morphologically abnormal structure true Inferred relationship Some 3
Ectodermal dysplasia, syndactyly and pili torti Associated morphology Morphologically abnormal structure true Inferred relationship Some 4
Ectodermal dysplasia, syndactyly and pili torti Finding site Nail unit structure true Inferred relationship Some 2
Ectodermal dysplasia, syndactyly and pili torti Pathological process Pathological developmental process true Inferred relationship Some 4
Ectodermal dysplasia, syndactyly and pili torti Pathological process Pathological developmental process true Inferred relationship Some 3
Ectodermal dysplasia, syndactyly and pili torti Finding site Tooth structure true Inferred relationship Some 3
Ectodermal dysplasia, syndactyly and pili torti Associated morphology Congenital anomaly false Inferred relationship Some
Ectodermal dysplasia, syndactyly and pili torti Associated morphology Congenital dysplasia false Inferred relationship Some 1
Ectodermal dysplasia, syndactyly and pili torti Associated morphology Congenital dysplasia false Inferred relationship Some 1
Ectodermal dysplasia, syndactyly and pili torti Finding site Skin structure false Inferred relationship Some 1
Ectodermal dysplasia, syndactyly and pili torti Associated morphology Dysplasia true Inferred relationship Some 1
Ectodermal dysplasia, syndactyly and pili torti Finding site Skin structure false Inferred relationship Some 1
Ectodermal dysplasia, syndactyly and pili torti Finding site Skin structure false Inferred relationship Some 2
Ectodermal dysplasia, syndactyly and pili torti Occurrence Congenital true Inferred relationship Some 2
Ectodermal dysplasia, syndactyly and pili torti Associated morphology Developmental abnormality false Inferred relationship Some 2
Ectodermal dysplasia, syndactyly and pili torti Occurrence Congenital false Inferred relationship Some
Ectodermal dysplasia, syndactyly and pili torti Is a Ectodermal dysplasia with hair-tooth-nail defects true Inferred relationship Some
Ectodermal dysplasia, syndactyly and pili torti Occurrence Congenital true Inferred relationship Some 3
Ectodermal dysplasia, syndactyly and pili torti Associated morphology Congenital dysplasia false Inferred relationship Some 3
Ectodermal dysplasia, syndactyly and pili torti Finding site Ectoderm structure false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

REPLACED BY association reference set

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