pseudohypoparathyroidism, nos

Preferred Label : pseudohypoparathyroidism, nos;

Details

Origin ID

DB-90850;

UMLS CUI

C0033806;

Automatic exact mappings (from CISMeF team)
- Albright disease [PASCAL descriptor]
- Albright hereditary osteodystrophy [ORDO Disease]
- Albright's Hereditary Osteodystrophy [NCIt concept]
- Polyostotic fibrous dysplasia of bone (disorder) [SNOMED CT concept]
- albright syndrome [MeSH concept]
- fibrous dysplasia, polyostotic [MeSH Descriptor]
Currated CISMeF NLP mapping
- Hypocalcemia [ICD-9 code]
- Hypoparathyroidism [MedDRA Preferred Term]
- Hypoparathyroidy [HRDO Sign]
- Parathyroid Hormone Resistance [NCIt concept]
- Pseudohypoparathyroidism [TUV Concept]
- Pseudohypoparathyroidism [TUV Term]
- Pseudohypoparathyroidism [ICD-10 Sub-category]
- Pseudohypoparathyroidism [PASCAL descriptor]
- Pseudohypoparathyroidism [NCIt concept]
- Pseudohypoparathyroidism [ICD-11 Subcategory]
- Pseudohypoparathyroidism [ICD-10 Sub-category (who)]
- Pseudohypoparathyroidism [MedDRA Preferred Term]
- Pseudohypoparathyroidism [HPO term]
- Pseudohypoparathyroidism [ORDO Disease]
- Pseudohypoparathyroidism (disorder) [SNOMED CT concept]
- pseudohypoparathyroidism [Disease (Nov.)]
- pseudohypoparathyroidism [DO Concept]
- pseudohypoparathyroidism [MeSH Descriptor]
- pseudohypoparathyroidism [MeSH concept]
False UMLS correspondences (reviewed by CISMeF team)
- Pseudohypoparathyroidism type I A (disorder) [SNOMED CT concept]
False automatic mappings
- Pseudohypoparathyroidism type I A (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Pseudohypoparathyroidism [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Pseudohypoparathyroidism type 1B [ORDO Disease]
- Pseudohypoparathyroidism type 2 [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Developmental anomaly of metabolic origin [ORDO Disease]
- Genetic dermis disorder [ORDO Disease]
- Genetic hypoparathyroidism [ORDO Disease]
- Genetic obesity [ORDO Disease]
- Genetic renal tubular disease [ORDO Disease]
- Musculoskeletal disease with cataract [ORDO Disease]
- Other dermis disorder [ORDO Disease]
- Rare hypoparathyroidism [ORDO Disease]
- Rare renal tubular disease [ORDO Disease]
- Syndrome with limb malformations as a major feature [ORDO Disease]
Metaterm(s)
- endocrinology [CISMeF Metaterm]
SNOMED CT concept
- Pseudohypoparathyroidism (disorder) [SNOMED CT concept]
See also inter- (CISMeF)
- hypoparathyroidism [Disease (Nov.)]
- pseudopseudohypoparathyroidism [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Pseudohypoparathyroidism [NCIt concept]
- Pseudohypoparathyroidism [ORDO Disease]
- Pseudohypoparathyroidism [ICD-10 Sub-category]
- Pseudohypoparathyroidism [HPO term]
- Pseudohypoparathyroidism [PASCAL descriptor]
- Pseudohypoparathyroidism [ICD-10 Sub-category (who)]
- Pseudohypoparathyroidism [MedDRA Preferred Term]
- Pseudohypoparathyroidism (disorder) [SNOMED CT concept]
- pseudohypoparathyroidism [MeSH concept]
- pseudohypoparathyroidism [Disease (Nov.)]
- pseudohypoparathyroidism [DO Concept]
- pseudohypoparathyroidism [MeSH Descriptor]
Validated automatic mappings to BTNT
- Pseudohypoparathyroidism with Albright hereditary osteodystrophy [ICD-11 More detail]

Keyword's position in hierarchy(ies) :

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