Osteoporosis, juvenile

Preferred Label : Osteoporosis, juvenile;

CISMeF acronym : IJO;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : IJO; Idiopathic juvenile osteoporosis;

Inheritance : Autosomal recessive;

Prefixed ID : 259750;

Details

Origin ID

259750;

UMLS CUI

C0264080;

Automatic exact mappings (from CISMeF team)
- Juvenile osteoporosis [PASCAL descriptor]
Currated CISMeF NLP mapping
- Feline osteogenesis imperfecta (disorder) [Inactive SNOMED CT concept]
- Idiopathic juvenile osteoporosis [ORDO Disease]
- Juvenile osteoporosis [MeSH concept]
- Pediatric Osteoporosis [NCIt concept]
- feline osteogenesis imperfecta [SNOMED Notion]
- idiopathic juvenile osteoporosis [DO Concept]
- juvenile osteoporosis [MeSH Supplementary Concept]
DO Cross reference
- idiopathic juvenile osteoporosis [DO Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Low serum calcitriol [HPO term]
- Osteoporosis [HPO term]
Not associated HPO term(s)
- Abnormal renal physiology [HPO term]
- Abnormal sclera morphology [HPO term]
- Decreased circulating calcifediol concentration [HPO term]
ORDO concept(s)
- Idiopathic juvenile osteoporosis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Feline osteogenesis imperfecta (disorder) [Inactive SNOMED CT concept]
- Idiopathic juvenile osteoporosis [ORDO Disease]
- Idiopathic juvenile osteoporosis [MedDRA Preferred Term]
- Juvenile osteoporosis [MeSH concept]
- Pediatric Osteoporosis [NCIt concept]
- feline osteogenesis imperfecta [SNOMED Notion]
- juvenile osteoporosis [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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