Abnormality of the kidney

Symptom Information:

Symptom ID: HPO:0000077
Kidney disease [HPO:0000077]
Renal anomalies [HPO:0000077]
Renal anomaly [HPO:0000077]
Renal anomalies [OMIM:Renal anomalies]
Renal anomaly [OMIM:Renal anomaly]
Renal anomalies (27%) [OMIM:Renal anomalies (27%)]
Renal anomalies (67% of patients) [OMIM:Renal anomalies (67% of patients)]
Renal anomalies (in some) [OMIM:Renal anomalies (in some)]
Renal anomalies (less common) [OMIM:Renal anomalies (less common)]
Renal anomalies (major) [OMIM:Renal anomalies (major)]
Cross references:
OMIM: "Renal anomalies" [OMIM:Renal anomalies]
OMIM: "Renal anomaly" [OMIM:Renal anomaly]
OMIM: "Renal anomalies (27%)" [OMIM:Renal anomalies (27%)]
OMIM: "Renal anomalies (67% of patients)" [OMIM:Renal anomalies (67% of patients)]
OMIM: "Renal anomalies (in some)" [OMIM:Renal anomalies (in some)]
OMIM: "Renal anomalies (less common)" [OMIM:Renal anomalies (less common)]
OMIM: "Renal anomalies (major)" [OMIM:Renal anomalies (major)]
Is a (Direct Parents):
HPO         Abnormality of the upper urinary tract
Is a (Whole tree): HPO:
    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)
Database Frequency: 73 / 7739

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
22q11.2 deletion syndrome (Orphanet:567)
AREDYLD syndrome (Orphanet:1133)
Acro-renal-ocular syndrome (Orphanet:959)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Alström syndrome (Orphanet:64)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
Autosomal dominant Robinow syndrome (Orphanet:3107)
BNAR syndrome (Orphanet:217266)
Baller-Gerold syndrome (Orphanet:1225)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 11 (OMIM:615988)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 13 (OMIM:615990)
Bardet-Biedl syndrome 14 (OMIM:615991)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 4 (OMIM:615982)
Bardet-Biedl syndrome 5 (OMIM:615983)
Bardet-Biedl syndrome 6 (OMIM:605231)
Bardet-Biedl syndrome 7 (OMIM:615984)
Bardet-Biedl syndrome 8 (OMIM:615985)
Bardet-Biedl syndrome 9 (OMIM:615986)
Beckwith-Wiedemann syndrome due to 11p15 microdeletion (Orphanet:231127)
Beckwith-Wiedemann syndrome due to CDKN1C mutation (Orphanet:231120)
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 (Orphanet:231117)
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 (Orphanet:96193)
Bohring-Opitz syndrome (Orphanet:97297)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carnitine palmitoyl transferase II deficiency (Orphanet:157)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Cockayne syndrome (Orphanet:191)
Cowden syndrome (Orphanet:201)
Ellis Van Creveld syndrome (Orphanet:289)
Erdheim-Chester disease (Orphanet:35687)
Familial dysautonomia (Orphanet:1764)
Familial supernumerary nipples (Orphanet:2456)
Gorlin syndrome (Orphanet:377)
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation (Orphanet:324525)
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome (Orphanet:363694)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Idiopathic hypereosinophilic syndrome (Orphanet:3260)
Infantile myofibromatosis (Orphanet:2591)
Joubert syndrome 28 (OMIM:617121)
Juvenile polyposis syndrome (Orphanet:2929)
Linear verrucous nevus syndrome (Orphanet:2611)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Monosomy 5p (Orphanet:281)
Mowat-Wilson syndrome (Orphanet:2152)
Nephronophthisis 9 (OMIM:613824)
Noonan syndrome with multiple lentigines (Orphanet:500)
Okihiro syndrome (Orphanet:93293)
Opitz G/BBB syndrome (Orphanet:2745)
Porencephaly-microcephaly-bilateral congenital cataract syndrome (Orphanet:306547)
Postaxial acrofacial dysostosis (Orphanet:246)
Radio-renal syndrome (Orphanet:3015)
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion (Orphanet:353281)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Scalp-ear-nipple syndrome (Orphanet:2036)
Thanatophoric dysplasia (Orphanet:2655)
Thanatophoric dysplasia type 1 (Orphanet:1860)
Thanatophoric dysplasia type 2 (Orphanet:93274)
Transaldolase deficiency (Orphanet:101028)
Trisomy 20p (Orphanet:261318)
Von Hippel-Lindau disease (Orphanet:892)
Von Voss-Cherstvoy syndrome (Orphanet:3439)
Waardenburg syndrome type 2 (Orphanet:895)
Wolf-Hirschhorn syndrome (Orphanet:280)
Wolfram syndrome 1 (OMIM:222300)
Zunich-Kaye syndrome (Orphanet:3474)