46762-1
Congenital hypothyroidism newborn screen interpretation
Active
Part Description
LP56766-6 Congenital hypothyroidism
A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA.
Source: National Library of Medicine, MeSH 2006
Fully-Specified Name
- Component
- Congenital hypothyroidism
- Property
- Imp
- Time
- Pt
- System
- Bld.dot
- Scale
- Nom
- Method
Additional Names
- Short Name
- CH DBS-Imp
- Display Name
- Congenital hypothyroidism (DBS) [Interp]
- Consumer Name Alpha Get Info
- Congenital hypothyroidism, Dried blood spot
Preferred Answer List: LL840-0
Source: Regenstrief Institute| Answer | Code | Score | Answer ID |
|---|---|---|---|
| In range | LA18592-8 | ||
| Borderline | LA4259-3 | ||
| IndeterminateCopyright http://snomed.info/sct ID:82334004 Indeterminate (qualifier value) | LA11884-6 | ||
| Out of range | LA18593-6 | ||
| Out of range requiring further dried blood spot testing for at least one condition | LA12430-7 | ||
| Out of range requiring immediate referral | LA25817-0 | ||
| Out of range requiring immediate second-tier testing for at least one condition | LA12431-5 | ||
| Out of range requiring deferred follow-up for at least one condition | LA18594-4 | ||
| One or more tests pending | LA16204-2 | ||
| Specimen unsatisfactory for at least one condition | LA16205-9 |
Basic Attributes
- Class
- CHEM
- Type
- Laboratory
- First Released
- Version 2.19
- Last Updated
- Version 2.73
- Change Reason
- Changed answer list from "Normative" to "Preferred" to fit the current LOINC model.
- Order vs. Observation
- Observation
- Common Test Rank Get Info
- 14221
Member of these Panels
| LOINC | Long Common Name |
|---|---|
| 54076-5 | Endocrine newborn screening panel |
| 54075-7 | Endocrine newborn screening panel (SI units) |
| 104191-2 | Guanidinoacetate methyltransferase (GAMT) deficiency newborn screening panel |
| 54089-8 | Newborn screening panel American Health Information Community (AHIC) |
| 54077-3 | Thyroid newborn screening panel (SI units) |
Member of these Groups Get Info
| LOINC Group | Group Name |
|---|---|
| LG18377-8 | Congenital hypothyroidism| |
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| es-ES | Spanish (Spain) | Hipotiroidismo Congenito: |
| es-MX | Spanish (Mexico) | Hipotiroidismo congénito: |
| fr-CA | French (Canada) | Hypothyroïdie congénitale: |
| fr-FR | French (France) | Hypothyroïdisme congénital: |
| fr-BE | French (Belgium) | Hypothyroïdie congénitale: |
| it-IT | Italian (Italy) | Ipotiroidismo congenito: Synonyms: Chimica Impressione/interpretazione di studio Punto nel tempo (episodio) Sangue Spot sangue secco |
| nl-NL | Dutch (Netherlands) | congenitale hypothyreoïdie: |
| pt-BR | Portuguese (Brazil) | Hipotireoidismo congênito: Synonyms: ; |
| ru-RU | Russian (Russian Federation) | Врождённый гипотиреоидизм: Synonyms: Впечатление/интерпретация исследования Кровь Кровь сухая капля Номинальный; |
| tr-TR | Turkish (Turkey) | Konjenital hipotiroizm: |
| zh-CN | Chinese (China) | 先天性甲状腺机能减退: Synonyms: CH; |
LOINC Terminology Service (API) using HL7® FHIR® Get Info
Requests to this service require a free LOINC username and password. Below is a sample of the possible capabilities. See the LOINC Terminology Service documentation for more information.
- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=46762-1
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LOINC Copyright
Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright