Unilateral renal agenesis
Symptom Information:
Symptom ID: | HPO:0000122 | ||||||
Synonyms: |
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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 hypoplasia/aplasia(HPO:0008678) Renal agenesis(HPO:0000104) Unilateral renal agenesis(HPO:0000122) MedDRA: |
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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) |