fibrous dysplasia, polyostotic

Preferred Label : fibrous dysplasia, polyostotic;

MeSH definition : FIBROUS DYSPLASIA OF BONE affecting several bones. When melanotic pigmentation (CAFE-AU-LAIT SPOTS) and multiple endocrine hyperfunction are additionally associated it is referred to as Albright syndrome.;

MeSH synonym : polyostotic fibrous dysplasias; polyostotic fibrous dysplasia; dysplasia, polyostotic fibrous; dysplasias, polyostotic fibrous; fibrous dysplasias, polyostotic;

MeSH hyponym : albrights syndrome; albright syndrome; Syndrome, Albright; McCune-Albright Syndrome; McCune Albright Syndrome; Syndrome, McCune-Albright; Albright's Disease; Fibrous Dysplasia with Pigmentary Skin Changes and Precocious Puberty; Albright's Syndrome with Precocious Puberty; Albright-Mccune-Sternberg Syndrome; Albright-Sternberg Syndrome; Albright's Syndrome; Syndrome, Albright's; Albright's Disease of Bone;

MeSH annotation : sometimes Jaffe-Lichtenstein (usually monostotic) goes here: check text; craniofacial fibrous dysplasia: coord IM with FACIAL BONES (IM) SKULL (IM);

Wikipedia link : https://en.wikipedia.org/wiki/Fibrous dysplasia, polyostotic;

Details

Origin ID

D005359;

UMLS CUI

C0016065;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Albright hereditary osteodystrophy [ORDO Disease]
- Albright's Hereditary Osteodystrophy [NCIt concept]
- McCune-Albright syndrome [ICD-11 More detail]
- Polyostotic fibrous dysplasia [ICD-11 More detail]
- Pseudohypoparathyroidism with Albright hereditary osteodystrophy [ICD-11 More detail]
- polyostotic fibrous dysplasia [Radlex concept]
- pseudohypoparathyroidism, nos [SNOMED Notion]
CISMeF manual mappings
- McCune-Albright syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- Albright disease [PASCAL descriptor]
- Albright disease [Disease (Nov.)]
- Albright's disease [MedDRA Preferred Term]
- Fibrous dysplasia of bone [PASCAL descriptor]
- McCune Albright syndrome [DO Concept]
- McCune-Albright Syndrome [NCIt concept]
- McCune-Albright syndrome [MedDRA LLT]
- Mccune-albright syndrome [OMIM Phenotype]
- Polyostotic Fibrous Dysplasia [NCIt concept]
- Polyostotic fibrous dysplasia [ICD-10 Sub-category]
- Polyostotic fibrous dysplasia [ICD-10 Sub-category (who)]
- Polyostotic fibrous dysplasia [HPO term]
- Polyostotic fibrous dysplasia [ORDO Disease]
- Polyostotic fibrous dysplasia of bone (disorder) [SNOMED CT concept]
- mccune-albright syndrome [SNOMED Notion]
- polyostotic fibrous dysplasia of bone, nos [SNOMED Notion]
DO Cross reference
- McCune Albright syndrome [DO Concept]
HPO term
- Polyostotic fibrous dysplasia [HPO term]
Manual NTBT mappings (CISMeF)
- Disease associated with non-acquired combined pituitary hormone deficiency [ORDO Disease]
- Genetic dermis disorder [ORDO Disease]
- Genetic hyperpigmentation of the skin [ORDO Disease]
- Genetic obesity [ORDO Disease]
- Hyperpigmentation of the skin [ORDO Disease]
- Musculoskeletal disease with cataract [ORDO Disease]
- Non-chondrodysplastic malformation syndrome affecting bones [ORDO Disease]
- Other dermis disorder [ORDO Disease]
- Polymalformative genetic syndrome with increased risk of developing cancer [ORDO Disease]
- Primary bone dysplasia with disorganized development of skeletal components [ORDO Disease]
- Rare peripheral precocious puberty [ORDO Disease]
- Syndrome with limb malformations as a major feature [ORDO Disease]
ORDO relation(s)
- McCune-Albright syndrome [ORDO Disease]
- Polyostotic fibrous dysplasia [ORDO Disease]
Record concept(s)
- albright syndrome [MeSH concept]
- fibrous dysplasia, polyostotic [MeSH concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Albright disease [PASCAL descriptor]
- McCune Albright syndrome [DO Concept]
- Polyostotic Fibrous Dysplasia [NCIt concept]
- Polyostotic fibrous dysplasia [ORDO Disease]
- Polyostotic fibrous dysplasia [ICD-10 Sub-category]
- Polyostotic fibrous dysplasia [HPO term]
- Polyostotic fibrous dysplasia [ICD-10 Sub-category (who)]
- Polyostotic fibrous dysplasia of bone [MedDRA LLT]
- Polyostotic fibrous dysplasia of bone [ICD-9 code]
- Polyostotic fibrous dysplasia of bone (disorder) [SNOMED CT concept]
- polyostotic fibrous dysplasia of bone, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- McCune Albright syndrome (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients