hypertryptophanemia, familial

Preferred Label : hypertryptophanemia, familial;

MeSH synonym : Hypertryptophanemia;

Origin ID

C563467;

UMLS CUI

C2931837;

Automatic exact mappings (from CISMeF team)
- Hypertryptophanemia [HPO term]
- familial hypertryptophanemia [DO Concept]
Currated CISMeF NLP mapping
- Familial hypertryptophanemia (disorder) [SNOMED CT concept]
- Hypertryptophanemia [OMIM Phenotype]
- Hypertryptophanemia [ORDO Disease]
DO Cross reference
- familial hypertryptophanemia [DO Concept]
MeSH term(s) associated for indexing
- amino acid metabolism, inborn errors [MeSH Descriptor]
Record concept(s)
- hypertryptophanemia, familial [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hypertryptophanemia (disorder) [SNOMED CT concept]
- Hypertryptophanemia [ORDO Disease]
- Hypertryptophanemia [OMIM Phenotype]
- familial hypertryptophanemia [DO Concept]