Abnormality of the kidney
Symptom Information:
Symptom ID: | HPO:0000077 | ||||||||||
Synonyms: |
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Quality: | |||||||||||
Cross references: |
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Is a (Direct Parents): |
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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) MedDRA: |
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Database Frequency: | 73 / 7739 | ||||||||||
Resource: |
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) |
BRANCHIOOTORENAL SYNDROME 1 | (OMIM:113650) |
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) |
SCHIZOPHRENIA 1 | (OMIM:181510) |
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) |