Renal agenesis

Symptom Information:

Symptom ID: HPO:0000104
Synonyms:
Absent kidney [HPO:0000104]
Renal aplasia [HPO:0000104]
Kidney agenesis [Orphanet:37080]
Renal agenesis (disorder) [Orphanet:37080]
Congenital hypoplasia of kidney (disorder) [Orphanet:37080]
Congenital hypoplasia of kidney [Orphanet:37080]
Congenital absence of kidney [Orphanet:37080]
Congenital absence of kidneys syndrome [Orphanet:37080]
Absent kidney [OMIM:Absent kidney]
Renal agenesis [OMIM:Renal agenesis]
Renal aplasia [OMIM:Renal aplasia]
Agenesis/hypoplasia/aplasia of kidneys [Orphanet:37080]
Renal agenesis congenital [Orphanet:37080]
Renal aplasia [Orphanet:37080]
Renal agenesis [Orphanet:37080]
Renal hypoplasia [Orphanet:37080]
Renal aplasia [MedDRA:10064655]
Congenital renal dysgenesis [MedDRA:10064655]
Renal agenesis [MedDRA:10064655]
Renal agenesis and dysgenesis [MedDRA:10064655]
Renal agenesis congenital [MedDRA:10064655]
Renal dysgenesis [MedDRA:10064655]
Unilateral renal agenesis [MedDRA:10064655]
Renal hypoplasia [MedDRA:10049102]
Congenital small kidney [MedDRA:10049102]
Absent kidneys [OMIM:Absent kidneys]
Renal agenesis (in some patients) [OMIM:Renal agenesis (in some patients)]
Renal agenesis, unilateral [OMIM:Renal agenesis, unilateral]
Renal agenesis, unilateral (1 patient) [OMIM:Renal agenesis, unilateral (1 patient)]
Renal agenesis, unilateral (in some patients) [OMIM:Renal agenesis, unilateral (in some patients)]
Renal agenesis/dysgenesis [OMIM:Renal agenesis/dysgenesis]
Renal aplasia (less common) [OMIM:Renal aplasia (less common)]
Renal hypoplasia (1 patient) [OMIM:Renal hypoplasia (1 patient)]
Renal hypoplasia (less common) [OMIM:Renal hypoplasia (less common)]
Renal hypoplasia (rare) [OMIM:Renal hypoplasia (rare)]
Quality:
Cross references:
HPO:0000089 "Renal hypoplasia" [Orphanet:37080]
HPO:0010958 "Bilateral renal agenesis" [Orphanet:37080]
Orphanet:37080 "Agenesis/hypoplasia/aplasia of kidneys" [Orphanet:37080]
OMIM: "Absent kidney" [OMIM:Absent kidney]
OMIM: "Renal agenesis" [OMIM:Renal agenesis]
OMIM: "Renal aplasia" [OMIM:Renal aplasia]
OMIM: "Absent kidneys" [OMIM:Absent kidneys]
OMIM: "Renal agenesis (in some patients)" [OMIM:Renal agenesis (in some patients)]
OMIM: "Renal agenesis, unilateral" [OMIM:Renal agenesis, unilateral]
OMIM: "Renal agenesis, unilateral (1 patient)" [OMIM:Renal agenesis, unilateral (1 patient)]
OMIM: "Renal agenesis, unilateral (in some patients)" [OMIM:Renal agenesis, unilateral (in some patients)]
OMIM: "Renal agenesis/dysgenesis" [OMIM:Renal agenesis/dysgenesis]
OMIM: "Renal aplasia (less common)" [OMIM:Renal aplasia (less common)]
OMIM: "Renal hypoplasia (1 patient)" [OMIM:Renal hypoplasia (1 patient)]
OMIM: "Renal hypoplasia (less common)" [OMIM:Renal hypoplasia (less common)]
OMIM: "Renal hypoplasia (rare)" [OMIM:Renal hypoplasia (rare)]
UMLS:C0266295 "Congenital hypoplasia of kidney" [Orphanet:37080]
UMLS:C0542519 "Congenital absence of kidney" [Orphanet:37080]
UMLS:C1609433 "Congenital absence of kidneys syndrome" [Orphanet:37080]
Is a (Direct Parents):
MedDRA Renal structural abnormalities and trauma
MedDRA Renal disorders NEC
HPO         Renal hypoplasia/aplasia
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 hypoplasia/aplasia(HPO:0008678)
                         Renal agenesis(HPO:0000104)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Renal structural abnormalities and trauma(MedDRA:10038529)
          Renal agenesis(HPO:0000104)
       Renal disorders NEC(MedDRA:10027695)
          Renal agenesis(HPO:0000104)
Database Frequency: 68 / 7739
Resource:

All diseases associated with this symptom:

AGONADISM, 46,XY, WITH MENTAL RETARDATION, SHORT STATURE, RETARDEDBONE AGE, AND MULTIPLE EXTRAGENITAL MALFORMATIONS (OMIM:600908)
Acro-renal-mandibular syndrome (Orphanet:958)
Acro-renal-ocular syndrome (Orphanet:959)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Autosomal recessive deafness-onychodystrophy syndrome (Orphanet:79500)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
BOR syndrome (Orphanet:107)
Bilateral renal agenesis (Orphanet:1848)
Branchio-oculo-facial syndrome (Orphanet:1297)
CHARGE syndrome (Orphanet:138)
CRYPTORCHIDISM, UNILATERAL OR BILATERAL (OMIM:219050)
Cantrell pentalogy (Orphanet:1335)
Carpenter-Waziri syndrome (Orphanet:93973)
Cat-eye syndrome (Orphanet:195)
Cenani-Lenz syndrome (Orphanet:3258)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Cloacal exstrophy (Orphanet:93929)
Coloboma of macula - brachydactyly type B (Orphanet:1471)
DIAMOND-BLACKFAN ANEMIA 11 (OMIM:614900)
Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type (Orphanet:363444)
Diabetic embryopathy (Orphanet:1926)
Double uterus - hemivagina - renal agenesis (Orphanet:3411)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
Emanuel syndrome (Orphanet:96170)
Exstrophy-epispadias complex (Orphanet:322)
FANCONI ANEMIA, COMPLEMENTATION GROUP A (OMIM:227650)
FANCONI ANEMIA, COMPLEMENTATION GROUP B (OMIM:300514)
FANCONI ANEMIA, COMPLEMENTATION GROUP C (OMIM:227645)
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 (OMIM:227646)
FANCONI ANEMIA, COMPLEMENTATION GROUP E (OMIM:600901)
Fanconi anemia (Orphanet:84)
Femoral-facial syndrome (Orphanet:1988)
Fryns syndrome (Orphanet:2059)
Goldenhar syndrome (Orphanet:374)
HYDRANENCEPHALY WITH RENAL APLASIA-DYSPLASIA (OMIM:236500)
Holmes-Gang syndrome (Orphanet:93970)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Holzgreve-Wagner-Rehder syndrome (Orphanet:2167)
Hypoparathyroidism - deafness - renal disease (Orphanet:2237)
Joubert syndrome with orofaciodigital defect (Orphanet:2754)
Juberg-Marsidi syndrome (Orphanet:93972)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
MURCS association (Orphanet:2578)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 1 (OMIM:249000)
Meckel syndrome, type 12 (OMIM:616258)
Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type (Orphanet:217026)
Neu-Laxova syndrome (Orphanet:2671)
OROFACIODIGITAL SYNDROME VI (OMIM:277170)
Okihiro syndrome (Orphanet:93293)
Radio-renal syndrome (Orphanet:3015)
Renal cysts and diabetes syndrome (Orphanet:93111)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Renpenning syndrome (Orphanet:3242)
SCHIZOPHRENIA 1 (OMIM:181510)
SERKAL syndrome (Orphanet:139466)
Scalp-ear-nipple syndrome (Orphanet:2036)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Smith-Lemli-Opitz syndrome (Orphanet:818)
THYMIC APLASIA WITH FETAL DEATH (OMIM:274210)
Tetraamelia - multiple malformations (Orphanet:3301)
Thymic-renal-anal-lung dysplasia (Orphanet:3326)
VACTERL/VATER association (Orphanet:887)
VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY (OMIM:602200)
VERHEIJ SYNDROME (OMIM:615583)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)