Tubular basement membrane disintegration

Symptom Information:

Symptom ID: HPO:0005583
Synonyms:
Disintegration of the tubular basement membrane [HPO:0005583]
Disintegration of the tubular basement membrane [OMIM:Disintegration of the tubular basement membrane]
Tubular basement membrane disintegration [OMIM:Tubular basement membrane disintegration]
Quality:
Cross references:
OMIM: "Disintegration of the tubular basement membrane" [OMIM:Disintegration of the tubular basement membrane]
OMIM: "Tubular basement membrane disintegration" [OMIM:Tubular basement membrane disintegration]
Is a (Direct Parents):
HPO         Abnormality of the renal tubule
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 nephron(HPO:0012575)
                         Abnormality of the renal tubule(HPO:0000091)
                            Tubular basement membrane disintegration(HPO:0005583)
MedDRA:
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant medullary cystic kidney disease with or without hyperuricemia (Orphanet:34149)
Autosomal recessive medullary cystic kidney disease (Orphanet:655)
MEDULLARY CYSTIC KIDNEY DISEASE 1 (OMIM:174000)
Nephronophthisis 1 (OMIM:256100)
Nephronophthisis 12 (OMIM:613820)
Nephronophthisis 13 (OMIM:614377)
Nephronophthisis 14 (OMIM:614844)
Nephronophthisis 15 (OMIM:614845)
Nephronophthisis 16 (OMIM:615382)
Nephronophthisis 18 (OMIM:615862)
Nephronophthisis 19 (OMIM:616217)
Nephronophthisis 2 (OMIM:602088)
Nephronophthisis 3 (OMIM:604387)
Nephronophthisis 4 (OMIM:606966)
Nephronophthisis 7 (OMIM:611498)
Nephronophthisis 9 (OMIM:613824)
Nephronophthisis-like nephropathy 1 (OMIM:613159)
Senior-Boichis syndrome (Orphanet:84081)