Renal hypoplasia/aplasia
Symptom Information:
Symptom ID: | HPO:0008678 | ||||||
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) MedDRA: |
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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-Küster-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) |