Nephronophthisis

Symptom Information:

Symptom ID: HPO:0000090
Synonyms:
juvenile nephronophthisis [HPO:0000090]
Juvenile nephronophthisis [OMIM:Juvenile nephronophthisis]
Nephronophthisis [OMIM:Nephronophthisis]
Nephronophthisis (1 patient) [OMIM:Nephronophthisis (1 patient)]
Nephronophthisis (less common) [OMIM:Nephronophthisis (less common)]
Nephronophthisis (rare) [OMIM:Nephronophthisis (rare)]
Quality:
Cross references:
OMIM: "Juvenile nephronophthisis" [OMIM:Juvenile nephronophthisis]
OMIM: "Nephronophthisis" [OMIM:Nephronophthisis]
OMIM: "Nephronophthisis (1 patient)" [OMIM:Nephronophthisis (1 patient)]
OMIM: "Nephronophthisis (less common)" [OMIM:Nephronophthisis (less common)]
OMIM: "Nephronophthisis (rare)" [OMIM:Nephronophthisis (rare)]
Is a (Direct Parents):
HPO         Abnormality of the renal medulla
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)
                         Nephronophthisis(HPO:0000090)
MedDRA:
Database Frequency: 42 / 7739
Resource:

All diseases associated with this symptom:

ARIMA SYNDROME (OMIM:243910)
Autosomal recessive medullary cystic kidney disease (Orphanet:655)
Cranioectodermal dysplasia 3 (OMIM:614099)
INTERSTITIAL NEPHRITIS, KARYOMEGALIC (OMIM:614817)
Joubert syndrome 15 (OMIM:614464)
Joubert syndrome 16 (OMIM:614465)
Joubert syndrome 2 (OMIM:608091)
Joubert syndrome 3 (OMIM:608629)
Joubert syndrome 4 (OMIM:609583)
Joubert syndrome 5 (OMIM:610188)
Joubert syndrome 6 (OMIM:610688)
Joubert syndrome 7 (OMIM:611560)
Joubert syndrome with hepatic defect (Orphanet:1454)
Joubert syndrome with ocular defect (Orphanet:220493)
Joubert syndrome with oculorenal defect (Orphanet:2318)
Joubert syndrome with renal defect (Orphanet:220497)
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 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)
RHYNS syndrome (Orphanet:140976)
Saldino-Mainzer syndrome (Orphanet:140969)
Senior-Boichis syndrome (Orphanet:84081)
Senior-Loken syndrome (Orphanet:3156)
Senior-Loken syndrome 1 (OMIM:266900)
Senior-Loken syndrome 3 (OMIM:606995)
Senior-Loken syndrome 4 (OMIM:606996)
Senior-Loken syndrome 5 (OMIM:609254)
Senior-Loken syndrome 6 (OMIM:610189)
Senior-Loken syndrome 7 (OMIM:613615)
Senior-Loken syndrome 8 (OMIM:616307)
Senior-Loken syndrome 9 (OMIM:616629)
Short-rib thoracic dysplasia 10 with or without polydactyly (OMIM:615630)