Analbuminemia - CISMeF

Preferred Label : Analbuminemia;

Symbol : ANALBA;

CISMeF acronym : ANALBA;

Type : Phenotype, molecular basis known;

Prefixed ID : #616000;

Details

Origin ID

616000;

UMLS CUI

C0878666;

Automatic exact mappings (from CISMeF team)
- Congenital analbuminemia [ORDO Disease]
Currated CISMeF NLP mapping
- Analbuminemia [NCIt concept]
- Analbuminemia (finding) [SNOMED CT concept]
Genes related to phenotype
- Albumin [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Edema [HPO term]
- Elevated circulating transferrin concentration [HPO term]
- Fatigue [HPO term]
- Global developmental delay [HPO term]
- Hypercholesterolemia [HPO term]
- Hypoalbuminemia [HPO term]
- Hypotension [HPO term]
- Increased LDL cholesterol concentration [HPO term]
- Lipodystrophy [HPO term]
- Oligohydramnios [HPO term]
- Osteoporosis [HPO term]
- Patent ductus arteriosus [HPO term]
- Recurrent lower respiratory tract infections [HPO term]
ORDO concept(s)
- Congenital analbuminemia [ORDO Disease]
See also inter- (CISMeF)
- Familial dysalbuminemic hyperthyroxinemia [ORDO Disease]
- Familial dysalbuminemic hyperthyroxinemia [PASCAL descriptor]
Semantic type(s)
- Finding [UMLS semantic type]
UMLS correspondences (same concept)
- Analbuminemia [NCIt concept]
- Analbuminemia (finding) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients