Version 2.78

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).
Source: Regenstrief LOINC

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

Fully-Specified Name

Component
Systemic findings and diseases associated with ophthalmological condition
Property
Prid
Time
Pt
System
^Patient
Scale
Nom
Method

Additional Names

Short Name
System find + dis assoc w ophth cond

Preferred Answer List: LL3739-1

Source: National Eye Institute
Answer Code Score Answer ID
NoneCopyright http://snomed.info/sct ID:260413007 None (qualifier value)

Screen time

 0 LA137-2
Ataxia 1 LA24636-5
Autism 2 LA24638-1
Cardiac defect(s) 3 LA24650-6
Cleft lip or palate 4 LA24660-5
CSF protein (>100mg/dl) 5 LA24682-9
Decreased bone density 6 LA24691-0
Delayed motor milestones 7 LA24693-6
Dementia 8 LA20372-1
Pediatric: Developmental delay 9 LA22265-5
Diabetes mellitus 10 LA14291-1
Dystonia 11 LA24705-8
Esophageal defect(s) 12 LA24714-0
Facial weakness 13 LA24720-7
Gastrointestinal defect(s) 14 LA24730-6
Gastrointestinal symptoms, recurrent 15 LA24731-4
Genitourinary defect(s) 16 LA24733-0
Headache, recurrent 17 LA24741-3
Hearing defect(s) 18 LA24742-1
Hypotonia 19 LA24751-2
Intellectual disabilities 20 LA24759-5
Klippel-feil 21 LA24771-0
Learning disability 22 LA24778-5
Limb malformations 23 LA24785-0
Limb weakness 24 LA24786-8
Myoclonus 25 LA24801-5
Pigmentation of skin different from other family members 26 LA24851-0
Polydactyly (digit abnormalities), Specify: 27 LA25437-7
Renal defect(s) 28 LA24872-6
Renal tubular dysfunction (Fanconi type) 29 LA24873-4
Scoliosis 30 LA22278-8
Seizures (history of, or treated) 31 LA24892-4
Short stature 32 LA24894-0
Skeletal defect(s) 33 LA24895-7
Stroke-like episodes associated with seizures 34 LA24908-8
Teeth defect(s) 35 LA24922-9
Umbilical abnormalities 36 LA24936-9
Other, Specify: OTH LA46-8
Unknown, Specify:Copyright http://snomed.info/sct ID:261665006 Unknown (qualifier value) UNK LA4489-6

Basic Attributes

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

Language Variants Get Info

Tag Language Translation
es-MX Spanish (Mexico) Hallazgos sistémicos y enfermedades asociadas a la afección oftalmológica:Tipo:Punto temporal:^ Paciente:Nominal:
it-IT Italian (Italy) Reperti sistemici e malattie associate a patologia oftalmologica:Prid:Pt:^Paziente:Nom:
Synonyms: Concetti storia NEI eyeGENE Occhio paziente Presenza o Identità Punto nel tempo (episodio)
zh-CN Chinese (China) 与眼科疾病相关联的全身性发现与疾病:存在与否或特征标识:时间点:^患者:名义型:
Synonyms: 与（和、跟）眼科（眼科学、眼部、眼睛）疾病（病、病症、疾患）相关联（相关、有关、相联系、有联系、存在联系）的全身性（系统性、涉及全系统的、影响全身的、系统性的）发现（所见）与疾病（病、病症、疾患、状况、状态、情况、健康状况、健康状态、健康情况） 健康状况;疾病;情况;病情;状态;条件 关联的 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 存在;存在与否;特征标识;身份;身份标识 时刻;随机;随意;瞬间 有联系的 相关的 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=79760-5