Bilateral renal agenesis

Symptom Information:

Symptom ID: HPO:0010958
Synonyms:
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]
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]
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:0000104 "Renal agenesis" [Orphanet:37080]
Orphanet:37080 "Agenesis/hypoplasia/aplasia of kidneys" [Orphanet:37080]
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
HPO         Renal agenesis
MedDRA Renal disorders NEC
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)
                            Bilateral renal agenesis(HPO:0010958)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Renal disorders NEC(MedDRA:10027695)
          Bilateral renal agenesis(HPO:0010958)
       Renal structural abnormalities and trauma(MedDRA:10038529)
          Bilateral renal agenesis(HPO:0010958)
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive deafness-onychodystrophy syndrome (Orphanet:79500)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Carpenter-Waziri syndrome (Orphanet:93973)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type (Orphanet:363444)
Holmes-Gang syndrome (Orphanet:93970)
Hypoparathyroidism - deafness - renal disease (Orphanet:2237)
Juberg-Marsidi syndrome (Orphanet:93972)
Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type (Orphanet:217026)
Renal cysts and diabetes syndrome (Orphanet:93111)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Renpenning syndrome (Orphanet:3242)
Scalp-ear-nipple syndrome (Orphanet:2036)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Thymic-renal-anal-lung dysplasia (Orphanet:3326)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)