polycystic kidneys, severe infantile with tuberous sclerosis

Preferred Label : polycystic kidneys, severe infantile with tuberous sclerosis;

MeSH note : PKDTS not included;

CISMeF synonym : PKDTS; tuberous sclerosis/polycystic kidney disease contiguous gene syndrome;

MeSH synonym : polycystic kidney disease, infantile severe, with tuberous sclerosis; Tuberous sclerosis-polycystic kidney disease contiguous gene syndrome;

Details

Origin ID

C536328;

UMLS CUI

C1838327;

Currated CISMeF NLP mapping
- Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis [ICD-11 More detail]
- Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis [ORDO Disease]
- Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (disorder) [SNOMED CT concept]
- Polycystic Kidney Disease, Infantile Severe, with Tuberous Sclerosis [NCIt concept]
- Polycystic kidney disease, infantile severe, with tuberous sclerosis [OMIM Phenotype]
MeSH term(s) associated for indexing
- polycystic kidney, autosomal recessive [MeSH Descriptor]
- tuberous sclerosis [MeSH Descriptor]
Record concept(s)
- Polycystic kidneys, severe infantile with tuberous sclerosis [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis [ORDO Disease]
- Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis [ICD-11 More detail]
- Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (disorder) [SNOMED CT concept]
- Polycystic Kidney Disease, Infantile Severe, with Tuberous Sclerosis [NCIt concept]
- Polycystic kidney disease, infantile severe, with tuberous sclerosis [OMIM Phenotype]

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