Renal hypoplasia/aplasia

Symptom Information:

Symptom ID: HPO:0008678
Synonyms:
Renal agenesis/hypoplasia [HPO:0008678]
Renal aplasia/hypoplasia [HPO:0008678]
Renal agenesis/hypoplasia [OMIM:Renal agenesis/hypoplasia]
Renal aplasia/hypoplasia [OMIM:Renal aplasia/hypoplasia]
Renal hypoplasia/aplasia [OMIM:Renal hypoplasia/aplasia]
Renal agenesis/hypoplasia (in some patients) [OMIM:Renal agenesis/hypoplasia (in some patients)]
Quality:
Cross references:
OMIM: "Renal agenesis/hypoplasia" [OMIM:Renal agenesis/hypoplasia]
OMIM: "Renal aplasia/hypoplasia" [OMIM:Renal aplasia/hypoplasia]
OMIM: "Renal hypoplasia/aplasia" [OMIM:Renal hypoplasia/aplasia]
OMIM: "Renal agenesis/hypoplasia (in some patients)" [OMIM:Renal agenesis/hypoplasia (in some patients)]
Is a (Direct Parents):
HPO         Abnormal renal morphology
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)
MedDRA:
Database Frequency: 127 / 7739
Resource:

All diseases associated with this symptom:

12q14 microdeletion syndrome (Orphanet:94063)
14q22q23 microdeletion syndrome (Orphanet:264200)
17q12 microdeletion syndrome (Orphanet:261265)
1q44 microdeletion syndrome (Orphanet:238769)
22q11.2 deletion syndrome (Orphanet:567)
46,XX disorder of sex development - anorectal anomalies (Orphanet:2973)
49,XXXXY syndrome (Orphanet:96264)
Acro-pectoro-renal dysplasia (Orphanet:956)
Acro-renal-mandibular syndrome (Orphanet:958)
Acro-renal-ocular syndrome (Orphanet:959)
Acrofacial dysostosis, Rodriguez type (Orphanet:1788)
Acrorenal syndrome (Orphanet:971)
Alagille syndrome (Orphanet:52)
Aniridia - renal agenesis - psychomotor retardation (Orphanet:1064)
Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis (Orphanet:1112)
Autosomal recessive polycystic kidney disease (Orphanet:731)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
BOR syndrome (Orphanet:107)
BRESEK syndrome (Orphanet:85284)
Bartsocas-Papas syndrome (Orphanet:1234)
Bilateral renal agenesis (Orphanet:1848)
Braddock syndrome (Orphanet:52047)
Brain malformation - congenital heart disease - postaxial polydactyly (Orphanet:75389)
Branchio-oculo-facial syndrome (Orphanet:1297)
C syndrome (Orphanet:1308)
CHILD syndrome (Orphanet:139)
CLOVE syndrome (Orphanet:140944)
Cantrell pentalogy (Orphanet:1335)
Cardiocranial syndrome, Pfeiffer type (Orphanet:2872)
Cat-eye syndrome (Orphanet:195)
Caudal duplication (Orphanet:1756)
Caudal regression sequence (Orphanet:3027)
Cenani-Lenz syndrome (Orphanet:3258)
Cerebro-reno-digital syndrome (Orphanet:1396)
Cloacal exstrophy (Orphanet:93929)
Coffin-Siris syndrome (Orphanet:1465)
Coloboma of macula - brachydactyly type B (Orphanet:1471)
Congenital unilateral hypoplasia of depressor anguli oris (Orphanet:1166)
Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis (Orphanet:171839)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Deafness - onychodystrophy (Orphanet:3231)
Desmosterolosis (Orphanet:35107)
Diabetic embryopathy (Orphanet:1926)
Diffuse neonatal hemangiomatosis (Orphanet:2123)
Distal 22q11.2 microduplication syndrome (Orphanet:261337)
Distal limb deficiencies - micrognathia syndrome (Orphanet:1307)
Distal monosomy 13q (Orphanet:1590)
Double uterus - hemivagina - renal agenesis (Orphanet:3411)
Down syndrome (Orphanet:870)
EEC syndrome (Orphanet:1896)
Ellis Van Creveld syndrome (Orphanet:289)
Familial caudal dysgenesis (Orphanet:1768)
Fanconi anemia (Orphanet:84)
Femoral-facial syndrome (Orphanet:1988)
Fibulo-ulnar hypoplasia - renal anomalies (Orphanet:2256)
Focal dermal hypoplasia (Orphanet:2092)
Fraser syndrome (Orphanet:2052)
Goldenhar syndrome (Orphanet:374)
Gonadal dysgenesis, XY type - associated anomalies (Orphanet:1770)
Hirschsprung disease - deafness - polydactyly (Orphanet:2155)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Holoprosencephaly - radial heart renal anomalies (Orphanet:3186)
Holzgreve-Wagner-Rehder syndrome (Orphanet:2167)
Hypoparathyroidism - deafness - renal disease (Orphanet:2237)
Isolated Klippel-Feil syndrome (Orphanet:2345)
Kabuki syndrome (Orphanet:2322)
Kallmann syndrome (Orphanet:478)
Kallmann syndrome - heart disease (Orphanet:2326)
Kousseff syndrome (Orphanet:2351)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Lethal chondrodysplasia, Moerman type (Orphanet:1420)
Lethal hemolytic anemia - genital anomalies (Orphanet:1046)
Limb body wall complex (Orphanet:2369)
MICROPHTHALMIA, SYNDROMIC 1 (OMIM:309800)
MURCS association (Orphanet:2578)
Marden-Walker syndrome (Orphanet:2461)
Matthew-Wood syndrome (Orphanet:2470)
Mayer-Rokitansky-K├╝ster-Hauser syndrome (Orphanet:3109)
McKusick-Kaufman syndrome (Orphanet:2473)
Micrencephaly - corpus callosum agenesis - abnormal genitalia (Orphanet:2508)
Microcephaly - cardiac defect - lung malsegmentation (Orphanet:2516)
Microgastria - limb reduction defect (Orphanet:2538)
Microphthalmia, Lenz type (Orphanet:568)
Morse-Rawnsley-Sargent syndrome (Orphanet:2570)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
Nager syndrome (Orphanet:245)
Neurocutaneous melanocytosis (Orphanet:2481)
Neurofaciodigitorenal syndrome (Orphanet:2673)
Oculoauriculovertebral spectrum with radial defects (Orphanet:2549)
Okamoto syndrome (Orphanet:2729)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Osteocraniostenosis (Orphanet:2763)
Otofaciocervical syndrome (Orphanet:2792)
PAGOD syndrome (Orphanet:991)
PELVIS syndrome (Orphanet:83628)
Pallister-Hall syndrome (Orphanet:672)
Peters-plus syndrome (Orphanet:709)
Poland syndrome (Orphanet:2911)
Premature chromosome condensation with microcephaly and intellectual deficit (Orphanet:52183)
Radio-renal syndrome (Orphanet:3015)
Renal coloboma syndrome (Orphanet:1475)
Renal cysts and diabetes syndrome (Orphanet:93111)
Renal dysplasia - megalocystis - sirenomelia (Orphanet:1850)
Renal-genital-middle ear anomalies (Orphanet:1092)
Ring chromosome 10 (Orphanet:1438)
Schisis association (Orphanet:63862)
Short rib-polydactyly syndrome (Orphanet:1505)
Short stature - wormian bones - dextrocardia (Orphanet:2863)
Sirenomelia (Orphanet:3169)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
Spondylocostal dysostosis - anal and genitourinary malformations (Orphanet:94095)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
Syndromic X-linked ichthyosis (Orphanet:281090)
Tetraploidy (Orphanet:3305)
Thomas syndrome (Orphanet:3316)
Thymic-renal-anal-lung dysplasia (Orphanet:3326)
Trisomy 20p (Orphanet:261318)
Trisomy 5p (Orphanet:1742)
Trisomy X (Orphanet:3375)
Ulbright-Hodes syndrome (Orphanet:3404)
Ulnar-mammary syndrome (Orphanet:3138)
VACTERL with hydrocephalus (Orphanet:3412)
VACTERL/VATER association (Orphanet:887)
Van Regemorter-Pierquin-Vamos syndrome (Orphanet:3419)
Williams syndrome (Orphanet:904)