| Disease Browser
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Parent Node:
 Urogenital Abnormalities (D014564) |
..Starting node
.. Genitourinary Tract Anomalies (C564424)
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Child Nodes:
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Sister Nodes: |
..Allanson Pantzar McLeod syndrome (C537048)  1
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..ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
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..Atrioventricular Septal Defect with Blepharophimosis and Anal and Radial Defects (C563994)
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..B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations (C563745)
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..BEAULIEU-BOYCOTT-INNES SYNDROME (OMIM:613680)
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..Bladder Exstrophy (D001746) 1
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..Calabro syndrome (C537960)
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..Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly (C563936)
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..Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence (C563127)
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..Cryptorchidism (D003456) 12
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..Disorders of Sex Development (D012734) 107
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..DK Phocomelia Syndrome (C565618)
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..Duker Weiss Siber syndrome (C535719)
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..Epispadias (D004842) 1
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..Genitopatellar Syndrome (C565255)
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..Genitourinary Tract Anomalies (C564424)
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..Hand foot uterus syndrome (C535627)
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..Hemolytic Anemia, Lethal Congenital Nonspherocytic, with Genital and Other Abnormalities (C563935)
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..Hypospadias (D007021) 17
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..Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies (C564543)
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..Lissencephaly, X-Linked, 2 (C564563)
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..Microcephaly seizures genital hypoplasia (C537540)
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..Microphthalmia, Syndromic 6 (C566440)
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..Multicystic Dysplastic Kidney (D021782) 2
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..Myotubular Myopathy with Abnormal Genital Development (C564561)
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..Nephritis, Hereditary (D009394) 11
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..Nephrosis deafness urinary tract digital malformation (C536402)
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..Noduli Cutanei, Multiple, with Urinary Tract Abnormalities (C563512)
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..Omphalocele exstrophy imperforate anus (C537748)
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..Piepkorn Karp Hickok syndrome (C535774)
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..Popliteal Pterygium Syndrome (C562509)
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..Proud Syndrome (C563110)
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..Pyelectasis (D058536)
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..Renal Adysplasia (C563261)
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..Renal dysplasia - limb defects syndrome (C537754)
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..Renal, Genital, and Middle Ear Anomalies (C564849)
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..Retrocaval Ureter (D064749)
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..Robinow Syndrome, Autosomal Dominant (C562492)
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..Rosselli-Gulienetti Syndrome (C563117)
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..Split-Hand With Obstructive Uropathy, Spina Bifida, And Diaphragmatic Defects (C566662)
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..Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies (C564799)
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..Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations (C567475)
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..Ureter, Bifid Or Double (C566012)
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..Urinary Fistula (D014548) 2
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..Uterine Anomalies (C562565)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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