norman roberts lissencephaly syndrome

Preferred Label : norman roberts lissencephaly syndrome;

MeSH synonym : lissencephaly syndrome, Norman-Roberts type; lissencephaly 2;

Origin ID

C537848;

UMLS CUI

C0796089;

Automatic exact mappings (from CISMeF team)
- Microlissencephaly type A [ICD-11 More detail]
- Norman-Roberts syndrome [DO Concept]
Currated CISMeF NLP mapping
- Cobblestone lissencephaly [ORDO Disease]
- Lissencephaly 2 [OMIM Phenotype]
- Lissencephaly syndrome Norman Roberts type (disorder) [SNOMED CT concept]
- Lissencephaly syndrome, Norman-Roberts type [ORDO Disease]
- Lissencephaly type 2 [ICD-11 More detail]
- Type 2 lissencephaly (disorder) [SNOMED CT concept]
- Type II lissencephaly [HPO term]
- lissencephaly 2 [Disease (Nov.)]
DO Cross reference
- Norman-Roberts syndrome [DO Concept]
False automatic mappings
- Microlissencephaly [ORDO Disease]
MeSH term(s) associated for indexing
- lissencephaly [MeSH Descriptor]
ORDO relation(s)
- Lissencephaly syndrome, Norman-Roberts type [ORDO Disease]
Record concept(s)
- Norman Roberts lissencephaly syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Lissencephaly 2 [OMIM Phenotype]
- Lissencephaly syndrome Norman Roberts type (disorder) [SNOMED CT concept]
- Lissencephaly syndrome, Norman-Roberts type [ORDO Disease]
- Norman-Roberts syndrome [DO Concept]