Absence of renal corticomedullary differentiation

Symptom Information:

Symptom ID: HPO:0005564
Synonyms:
Absent renal corticomedullary differentiation [HPO:0005564]
Loss of corticomedullary differentiation [HPO:0005564]
Loss of corticomedullary differentiation [OMIM:Loss of corticomedullary differentiation]
Quality:
Cross references:
OMIM: "Loss of corticomedullary differentiation" [OMIM:Loss of corticomedullary differentiation]
Is a (Direct Parents):
HPO         Abnormal renal corticomedullary differentiation
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal morphology(HPO:0012210)
                      Abnormality of the renal medulla(HPO:0100957)
                         Abnormal renal corticomedullary differentiation(HPO:0005932)
                            Absence of renal corticomedullary differentiation(HPO:0005564)
                      Abnormality of the renal cortex(HPO:0011035)
                         Abnormal renal corticomedullary differentiation(HPO:0005932)
                            Absence of renal corticomedullary differentiation(HPO:0005564)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive polycystic kidney disease (Orphanet:731)
Nephronophthisis 2 (OMIM:602088)