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18077009: Trichorhinophalangeal syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
30539015 Trichorhinophalangeal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
401591000241118 syndrome tricho-rhino-phalangien (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
745453014 Trichorhinophalangeal syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
950061000172110 syndrome tricho-rhino-phalangien fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Trichorhinophalangeal syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Trichorhinophalangeal syndrome morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 2
Trichorhinophalangeal syndrome localisation d'une constatation (attribut) face true Inferred relationship Some 1
Trichorhinophalangeal syndrome morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
Trichorhinophalangeal syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Trichorhinophalangeal syndrome survenue (attribut) congénital true Inferred relationship Some 1
Trichorhinophalangeal syndrome morphologie associée (attribut) dysplasie false Inferred relationship Some 1
Trichorhinophalangeal syndrome est un(e) (attribut) Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Some
Trichorhinophalangeal syndrome est un(e) (attribut) Ectodermal dysplasia with hair-tooth-nail defects false Inferred relationship Some
Trichorhinophalangeal syndrome est un(e) (attribut) Acromesomelic dysplasia syndrome false Inferred relationship Some
Trichorhinophalangeal syndrome localisation d'une constatation (attribut) structure d'un membre false Inferred relationship Some 2
Trichorhinophalangeal syndrome morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Trichorhinophalangeal syndrome morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 1
Trichorhinophalangeal syndrome morphologie associée (attribut) Congenital malformation false Inferred relationship Some 3
Trichorhinophalangeal syndrome est un(e) (attribut) Disorder of soft tissue of limb false Inferred relationship Some
Trichorhinophalangeal syndrome localisation d'une constatation (attribut) structure osseuse false Inferred relationship Some 1
Trichorhinophalangeal syndrome morphologie associée (attribut) Congenital malformation false Inferred relationship Some 1
Trichorhinophalangeal syndrome localisation d'une constatation (attribut) Musculoskeletal structure of limb false Inferred relationship Some 3
Trichorhinophalangeal syndrome localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Trichorhinophalangeal syndrome morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 1
Trichorhinophalangeal syndrome morphologie associée (attribut) Congenital malformation false Inferred relationship Some 1
Trichorhinophalangeal syndrome localisation d'une constatation (attribut) structure d'un membre false Inferred relationship Some 1
Trichorhinophalangeal syndrome localisation d'une constatation (attribut) structure d'un membre false Inferred relationship Some 1
Trichorhinophalangeal syndrome survenue (attribut) congénital true Inferred relationship Some 2
Trichorhinophalangeal syndrome morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
Trichorhinophalangeal syndrome survenue (attribut) congénital false Inferred relationship Some 3
Trichorhinophalangeal syndrome morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 3
Trichorhinophalangeal syndrome localisation d'une constatation (attribut) structure d'un membre true Inferred relationship Some 2
Trichorhinophalangeal syndrome localisation d'une constatation (attribut) face false Inferred relationship Some 3
Trichorhinophalangeal syndrome survenue (attribut) congénital false Inferred relationship Some
Trichorhinophalangeal syndrome localisation d'une constatation (attribut) Skeletal system structure false Inferred relationship Some 1
Trichorhinophalangeal syndrome localisation d'une constatation (attribut) structure osseuse false Inferred relationship Some 1
Trichorhinophalangeal syndrome localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Trichorhinophalangeal syndrome morphologie associée (attribut) Developmental abnormality false Inferred relationship Some
Trichorhinophalangeal syndrome localisation d'une constatation (attribut) Musculoskeletal structure of limb false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Trichorhinophalangeal syndrome type 1 and 3 est un(e) (attribut) True Trichorhinophalangeal syndrome Inferred relationship Some
Trichorhinophalangeal dysplasia type III (disorder) est un(e) (attribut) True Trichorhinophalangeal syndrome Inferred relationship Some
Langer-Giedion syndrome est un(e) (attribut) True Trichorhinophalangeal syndrome Inferred relationship Some
Trichorhinophalangeal dysplasia type I est un(e) (attribut) True Trichorhinophalangeal syndrome Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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