All diseases

OMIM ID
191830
OMIM term:
RENAL ADYSPLASIA
Alternative terms:
RENAL AGENESIS
RENAL APLASIA
HEREDITARY RENAL APLASIA; HRA UROGENITAL ADYSPLASIA, INCLUDED
POTTER SYNDROME, INCLUDED
(∗) Location:
10q11.21   22q13.31  
(†) Associated OMIM genes:
RET   UPK3A  
(‡) Associated MGI genes:

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