osteopetrosis, mild autosomal recessive form

Preferred Label : osteopetrosis, mild autosomal recessive form;

MeSH note : Optb2 not included;

MeSH synonym : mild autosomal recessive form of osteopetrosis; osteopetrosis, autosomal recessive 2; osteopetrosis, Osteoclast-Poor;

Details

Origin ID

C536059;

UMLS CUI

C1850126;

Automatic exact mappings (from CISMeF team)
- Osteopetrosis, autosomal recessive 2 [OMIM Phenotype]
- autosomal recessive osteopetrosis 2 [DO Concept]
MeSH term(s) associated for indexing
- osteopetrosis [MeSH Descriptor]
Record concept(s)
- Osteopetrosis, mild autosomal recessive form [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Osteopetrosis, autosomal recessive 2 [OMIM Phenotype]
- autosomal recessive osteopetrosis 2 [DO Concept]

Keyword's position in hierarchy(ies) :

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