Unilateral renal agenesis

Symptom Information:

Symptom ID: HPO:0000122
Synonyms:
Unilateral kidney agenesis [HPO:0000122]
Unilateral kidney agenesis [OMIM:Unilateral kidney agenesis]
Unilateral renal agenesis [OMIM:Unilateral renal agenesis]
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)]
Quality:
Cross references:
OMIM: "Unilateral kidney agenesis" [OMIM:Unilateral kidney agenesis]
OMIM: "Unilateral renal agenesis" [OMIM:Unilateral renal agenesis]
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)]
Is a (Direct Parents):
HPO         Renal agenesis
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)
                            Unilateral renal agenesis(HPO:0000122)
MedDRA:
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
22q11.2 deletion syndrome (Orphanet:567)
Aniridia - renal agenesis - psychomotor retardation (Orphanet:1064)
Atypical Mayer-Rokitansky-Küster-Hauser syndrome (Orphanet:247768)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
BRESEK syndrome (Orphanet:85284)
Bladder exstrophy (Orphanet:93930)
Braddock syndrome (Orphanet:52047)
Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type (Orphanet:363444)
Diabetic embryopathy (Orphanet:1926)
HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA (OMIM:308700)
HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA (OMIM:244200)
Hirschsprung disease - deafness - polydactyly (Orphanet:2155)
Hypoparathyroidism - deafness - renal disease (Orphanet:2237)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Isolated Klippel-Feil syndrome (Orphanet:2345)
KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA (OMIM:308750)
LEOPARD SYNDROME 1 (OMIM:151100)
Microcephaly - cardiac defect - lung malsegmentation (Orphanet:2516)
Microgastria - limb reduction defect (Orphanet:2538)
Nager syndrome (Orphanet:245)
Neurofaciodigitorenal syndrome (Orphanet:2673)
Noonan syndrome with multiple lentigines (Orphanet:500)
Renal cysts and diabetes syndrome (Orphanet:93111)