Log In

Term Description

This term was developed in collaboration with the National Institute of Health's National Eye Institute (NEI) as part of an effort to standardize the data elements collected by the National Ophthalmic Disease Genotyping and Phenotyping Network (eyeGENE).

Part Description

LP203649-1   EYE.HX.NEI
Developed in collaboration with the National Institute of Health's National Eye Institute (NEI) as part of an effort to standardize the data elements collected by the National Ophthalmic Disease Genotyping and Phenotyping Network (eyeGENE). Source: Regenstrief LOINC

LOINC Names Get Info

Fully-Specified Name
Congenital cranial dysinnervation syndrome (CCDS) suspected:Type:Pt:^Patient:Nom:
Long Common Name
Type of Congenital cranial dysinnervation syndrome (CCDS) suspected
Short Name
Type of CCDS susp

Part Model Get Info

  • Component
    Congenital cranial dysinnervation syndrome (CCDS) suspected
    LP201227-8
    • Analyte
      Congenital cranial dysinnervation syndrome (CCDS) suspected
      LP201227-8
      • Component Numerator
        Congenital cranial dysinnervation syndrome (CCDS) suspected
        LP201227-8
        • Component Numerator Core
          Congenital cranial dysinnervation syndrome (CCDS) suspected
          LP201227-8
        • Component Numerator Core Suffix
          NULL
           
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    Type
    LP6886-8
  • Time
    Pt
    LP6960-1
  • System
    ^Patient
    LP310005-6
    • System Core
      NULL
       
    • Super System
      Patient
      LP6985-8
  • Scale
    Nom
    LP7750-5
  • Method
    NULL
     

Preferred Answer List: LL3728-4

Source: National Eye Institute
AnswerCodeScoreAnswer ID
Congenital fibrosis of the extraocular muscles (CFEOM)1LA24668-8
Duane-radial ray syndrome2LA24703-3
Duane syndrome retraction3LA24702-5
Horizontal gaze palsy with progressive scoliosis (HGPPS)4LA24743-9
HOXA1 syndromes (BSAS and ABDS)5LA24744-7
Moebius syndrome6LA24796-7
Other, Specify:OTHLA46-8
UnknownCopyright http://snomed.info/sct ID:261665006 Unknown (qualifier value)UNKLA4489-6

Basic Attributes

Class
EYE.HX.NEI
Type
Clinical
First Released
Version 2.54
Last Updated
Version 2.54 (MIN)
Order vs. Observation
Observation

Language Variants Get Info

TagLanguageTranslation
el-GRGreek (Greece)Υποψία συνδρόμου συγγενούς διαταραχής κρανιακής δυσνεύρωσης (CCDS):Type:Pt:^Ασθενής:Nom:
Synonyms: - EYE EYE.HX EYE.HX.NEI Nom Pt Type Ασθενής Υποψία συνδρόμου συγγενούς διαταραχής κρανιακής δυσνεύρωσης (CCDS)
es-MXSpanish (Mexico)Sospecha de síndrome de desinervación craneal congénita (CCDS):Tipo:Punto temporal:^ Paciente:Nominal:
it-ITItalian (Italy)Sindrome da disinnervazione cranica congenita (CCDS) sospetta:Tipo:Pt:^Paziente:Nom:
Synonyms: Concetti storia NEI eyeGENE Occhio paziente Punto nel tempo (episodio)
zh-CNChinese (China)所怀疑的先天性颅神经发育异常综合征:类型:时间点:^患者:名义型:
Synonyms: 分类型应答;分类型结果;名义性;名称型;名词型;名词性;标称性;没有自然次序的名义型或分类型应答 医疗服务对象;客户;病人;病患;病号;超系统 - 病人 型 所怀疑的（疑似的、疑似）先天性颅神经发育异常综合征;Congenital cranial dysinnervation syndrome;CCDS;Congenital Cranial Dysinnervation Disorders;CCDDs 时刻;随机;随意;瞬间 眼;眼睛;眼科;眼科学与验光变量;眼科学与验光指标 眼科学与视力测定变量.病史（历史纪录、历史、病史纪录） 眼科学与视力测定变量.病史（眼科病史、眼睛病史、眼部病史、HX）.NEI;NEI eyeGENE''s eye history concepts;NEI eyeGENE 病史（眼科病史、眼睛病史、眼部病史、HX）概念

LOINC Terminology Service (API) using HL7® FHIR® Get Info

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=79736-5