Renal agenesis
Symptom Information:
Symptom ID: | HPO:0000104 | |||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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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) 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) |
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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) |