hypophosphatasia, perinatal lethal

Preferred Label : hypophosphatasia, perinatal lethal;

MeSH note : mutation in tissue-nonspecific alkaline phosphatase;

Origin ID

C567107;

UMLS CUI

C2673477;

Automatic exact mappings (from CISMeF team)
- Hypophosphatasia, infantile [OMIM Phenotype]
Currated CISMeF NLP mapping
- Perinatal lethal hypophosphatasia [ORDO Disease]
MeSH term(s) associated for indexing
- hypophosphatasia [MeSH Descriptor]
Record concept(s)
- hypophosphatasia, perinatal lethal [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Perinatal lethal hypophosphatasia [ORDO Disease]