Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
penile disease +     
physical disorder +     
Agenesis of Corpus Callosum with Facial Anomalies and Robin Sequence 
agnathia-otocephaly complex  
Allanson Pantzar McLeod Syndrome +   
Alport syndrome +   
anogenital venereal wart +   
Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis  
Atrioventricular Septal Defect with Blepharophimosis and Anal and Radial Defects 
B-Cell Immunodeficiency, Distal Limb Anomalies, and Urogenital Malformations 
balanitis +  
balanoposthitis 
Beaulieu-Boycott-Innes Syndrome  
Bifid or Double Ureter 
bladder exstrophy-epispadias-cloacal exstrophy complex +   
blepharophimosis, ptosis, and epicanthus inversus syndrome  
Calabro Syndrome 
Cardiac-Urogenital Syndrome  
chromosome 1p32-p31 deletion syndrome  
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
cleft palate-lateral synechia syndrome  
congenital nervous system abnormality +   
cryptorchidism +   
DK Phocomelia Syndrome 
Duker Weiss Siber syndrome 
Epispadias +   
Fraser syndrome +   
Fused Kidney  
gastroschisis +   
Genitopatellar Syndrome  
Genitourinary Tract Anomalies 
hand-foot-genital syndrome  
hypospadias +   
A birth defect due to malformation of the URETHRA in which the urethral opening is below its normal location. In the male, the malformed urethra generally opens on the ventral surface of the PENIS or on the PERINEUM. In the female, the malformed urethral opening is in the VAGINA.
IMAGe syndrome  
IMAGEI Syndrome  
imperforate anus +   
Klippel-Feil syndrome +   
Lethal Congenital Nonspherocytic Hemolytic Anemia with Genital and Other Abnormalities 
leukoplakia of penis 
Lissencephaly, X-Linked, 2  
Meckel's diverticulum 
Microcephaly Seizures Genital Hypoplasia 
Microphthalmia, Syndromic 6  
MORM Syndrome  
Multicystic Dysplastic Kidney +   
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
Myotubular Myopathy with Abnormal Genital Development 
Nephrosis Deafness Urinary Tract Digital Malformation 
neural tube defect +   
omphalocele  
Omphalocele Exstrophy Imperforate Anus 
orofacial cleft +   
penile neoplasm +   
Peyronie's disease  
phimosis +  
Piepkorn Karp Hickok syndrome 
Poland syndrome 
polydactyly +   
popliteal pterygium syndrome +   
priapism +   
Proteus syndrome +   
Proud Syndrome  
Pyelectasis 
radioulnar synostosis  
renal agenesis +   
Renal Dysplasia - Limb Defects Syndrome 
Renal, Genital, and Middle Ear Anomalies 
Retrocaval Ureter 
Robinow syndrome +   
Rosselli-Gulienetti Syndrome 
sex development disorder +   
Split-Hand with Obstructive Uropathy, Spina Bifida, and Diaphragmatic Defects 
Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies 
Structural Heart Defects and Renal Anomalies Syndrome  
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations  
Urinary Fistula +  
Uterine Anomalies 
visceral heterotaxy +   
Weaver syndrome  

Synonyms
Exact Synonyms: HYSP4 ;   familial hypospadias ;   hypospadia
Related Synonyms: Hypospadias 4, X-Linked, Susceptibility to
Primary IDs: MESH:D007021
Alternate IDs: DOID:9000084 ;   OMIM:300856 ;   RDO:0000276 ;   RDO:0010084
Xrefs: OMIM:PS300633 ;   ORDO:440
Definition Sources: MESH:D007021, http://en.wikipedia.org/wiki/Hypospadias, http://ghr.nlm.nih.gov/glossary=hypospadias

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.