renal hypodysplasia, nonsyndromic, 1

Preferred Label : renal hypodysplasia, nonsyndromic, 1;

Origin ID

C563661;

UMLS CUI

C1835826;

Currated CISMeF NLP mapping
- CAKUT1 [DO Concept]
- Congenital anomalies of kidney and urinary tract 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- kidney diseases [MeSH Descriptor]
Record concept(s)
- renal hypodysplasia, nonsyndromic, 1 [MeSH concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- CAKUT1 [DO Concept]
- Congenital anomalies of kidney and urinary tract 1 [OMIM Phenotype]