Osteopoikilosis and dacryocystitis

Preferred Label : Osteopoikilosis and dacryocystitis;

Type : Other, mainly phenotypes with suspected mendelian basis;

Description : Gunal et al. (1993) described 5 members of a family who had osteopoikilosis (166700) in association with dacryocystitis. Inheritance appeared to be autosomal dominant. Chromosome analysis showed normal karyotype in all patients. *FIELD* RF 1. Gunal, I.; Seber, S.; Basaran, N.; Artan, S.; Gunal, K.; Gokturk, E.: Dacryocystitis associated with osteopoikilosis. Clin. Genet. 44: 211-213, 1993. *FIELD* CS Skel: Osteopoikilosis;

Inheritance : Autosomal dominant;

Prefixed ID : 166705;

Details

Origin ID

166705;

UMLS CUI

C1833698;

Currated CISMeF NLP mapping
- Dacryocystitis - osteopoikilosis [ICD-11 More detail]
- Dacryocystitis and osteopoikilosis syndrome (disorder) [SNOMED CT concept]
- Dacryocystitis-osteopoikilosis syndrome [ORDO Disease]
- Osteopoikilosis and dacryocystitis [MeSH concept]
- osteopoikilosis and dacryocystitis [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Dacryocystitis [HPO term]
- Osteopoikilosis [HPO term]
ORDO concept(s)
- Dacryocystitis-osteopoikilosis syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dacryocystitis - osteopoikilosis [ICD-11 More detail]
- Dacryocystitis and osteopoikilosis syndrome (disorder) [SNOMED CT concept]
- Dacryocystitis-osteopoikilosis syndrome [ORDO Disease]
- Osteopoikilosis and dacryocystitis [MeSH concept]
- osteopoikilosis and dacryocystitis [MeSH Supplementary Concept]

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