Renal dysplasia
Symptom Information:
Symptom ID: | HPO:0000110 | |||||||||||||||
Synonyms: |
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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) Abnormal renal morphology(HPO:0012210) Renal dysplasia(HPO:0000110) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Renal structural abnormalities and trauma(MedDRA:10038529) Renal dysplasia(HPO:0000110) |
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Database Frequency: | 44 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
22q11.2 deletion syndrome | (Orphanet:567) |
Alagille syndrome due to 20p12 microdeletion | (Orphanet:261600) |
Alagille syndrome due to a JAG1 point mutation | (Orphanet:261619) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
BOR syndrome | (Orphanet:107) |
BRANCHIOOTORENAL SYNDROME 2 | (OMIM:610896) |
BRESEK syndrome | (Orphanet:85284) |
Bardet-Biedl syndrome | (Orphanet:110) |
Bardet-Biedl syndrome 8 | (OMIM:615985) |
Bilateral renal agenesis | (Orphanet:1848) |
CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION | (OMIM:601389) |
CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME | (OMIM:218650) |
Combined oxidative phosphorylation defect type 11 | (Orphanet:324535) |
Diabetic embryopathy | (Orphanet:1926) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 | (OMIM:129900) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
EEC syndrome | (Orphanet:1896) |
HYDRANENCEPHALY WITH RENAL APLASIA-DYSPLASIA | (OMIM:236500) |
HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED | (OMIM:241800) |
Hypoparathyroidism - deafness - renal disease | (Orphanet:2237) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
Lymphangioleiomyomatosis | (Orphanet:538) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 | (OMIM:236670) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 13 | (OMIM:615287) |
Megacystis-microcolon-intestinal hypoperistalsis syndrome | (Orphanet:2241) |
Micrencephaly - corpus callosum agenesis - abnormal genitalia | (Orphanet:2508) |
Multicystic renal dysplasia | (Orphanet:1851) |
Multiple congenital anomalies - hypotonia - seizures syndrome | (Orphanet:280633) |
Muscle-eye-brain disease | (Orphanet:588) |
OROFACIODIGITAL SYNDROME VI | (OMIM:277170) |
Pallister-Hall syndrome | (Orphanet:672) |
RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO | (OMIM:601331) |
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 | (OMIM:208540) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Renal-hepatic-pancreatic dysplasia | (Orphanet:294415) |
SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIB | (OMIM:615087) |
Saldino-Mainzer syndrome | (Orphanet:140969) |
Short-rib thoracic dysplasia 3 with or without polydactyly | (OMIM:613091) |
Tetrasomy 12p | (Orphanet:884) |
Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
Townes-Brocks syndrome | (Orphanet:857) |
Ulbright-Hodes syndrome | (Orphanet:3404) |
VACTERL/VATER association | (Orphanet:887) |