Renal dysplasia

Symptom Information:

Symptom ID: HPO:0000110
Synonyms:
Dysplastic kidneys [HPO:0000110]
Renal adysplasia [HPO:0000110]
Renal dysplasia (disorder) [Orphanet:37200]
Dysplastic kidneys [OMIM:Dysplastic kidneys]
Renal adysplasia [OMIM:Renal adysplasia]
Renal dysplasia [OMIM:Renal dysplasia]
Multicystic kidney/renal dysplasia [Orphanet:37200]
Renal dysplasia [Orphanet:37200]
Renal dysplasia [MedDRA:10038433]
Cell dysplasia kidney [MedDRA:10038433]
Congenital renal dysplasia NOS [MedDRA:10038433]
Dysplastic kidney [OMIM:Dysplastic kidney]
Dysplastic kidney (1 of 7 patients) [OMIM:Dysplastic kidney (1 of 7 patients)]
Dysplastic kidneys (1 patient) [OMIM:Dysplastic kidneys (1 patient)]
Renal dysplasia (WWS) [OMIM:Renal dysplasia (WWS)]
Quality:
Cross references:
HPO:0000003 "Multicystic kidney dysplasia" [Orphanet:37200]
HPO:0000113 "Polycystic kidney dysplasia" [Orphanet:37200]
Orphanet:37200 "Multicystic kidney/renal dysplasia" [Orphanet:37200]
OMIM: "Dysplastic kidneys" [OMIM:Dysplastic kidneys]
OMIM: "Renal adysplasia" [OMIM:Renal adysplasia]
OMIM: "Renal dysplasia" [OMIM:Renal dysplasia]
OMIM: "Dysplastic kidney" [OMIM:Dysplastic kidney]
OMIM: "Dysplastic kidney (1 of 7 patients)" [OMIM:Dysplastic kidney (1 of 7 patients)]
OMIM: "Dysplastic kidneys (1 patient)" [OMIM:Dysplastic kidneys (1 patient)]
OMIM: "Renal dysplasia (WWS)" [OMIM:Renal dysplasia (WWS)]
Is a (Direct Parents):
HPO         Abnormal renal morphology
Orphanet Multicystic kidney dysplasia
MedDRA Renal structural abnormalities and trauma
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)
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)