Bilateral renal agenesis
Symptom Information:
Symptom ID: | HPO:0010958 | |||||||||||||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) 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) |
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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) |