Pages that link to "Property:P78"
From determinar.ia.br - Determine suas informações
The following pages link to Knowledge Architect (P78):
Displaying 50 items.
- Unicornuate uterus (Q46377) (← links)
- Agenesis or aplasia of uterine body (Q46378) (← links)
- Bicornuate uterus (Q46379) (← links)
- Agenesis or aplasia of cervix (Q46380) (← links)
- Embryonic cyst of cervix (Q46381) (← links)
- Congenital fistulae between uterus and digestive and urinary tracts (Q46382) (← links)
- Absence of vagina (Q46383) (← links)
- Septate vagina (Q46384) (← links)
- Congenital rectovaginal fistula (Q46385) (← links)
- Imperforate hymen (Q46386) (← links)
- Fusion of labia (Q46387) (← links)
- Clitoromegaly (Q46388) (← links)
- Structural developmental anomalies of clitoris (Q46389) (← links)
- Agenesis of clitoris (Q46390) (← links)
- Duplication of clitoris (Q46391) (← links)
- Embryonic cyst of vulva (Q46392) (← links)
- Absence of vulva (Q46393) (← links)
- Structural developmental anomalies of vulva (Q46394) (← links)
- Cryptorchidism (Q46395) (← links)
- Ectopic testis (Q46396) (← links)
- Undescended testicle, unilateral (Q46397) (← links)
- Undescended testicle, bilateral (Q46398) (← links)
- Hypospadias, scrotal (Q46399) (← links)
- Hypospadias (Q46400) (← links)
- Hypospadias, balanic (Q46401) (← links)
- Hypospadias, coronal (Q46402) (← links)
- Hypospadias, glandular (Q46403) (← links)
- Hypospadias, penile (Q46404) (← links)
- Hypospadias, penoscrotal (Q46405) (← links)
- Hypospadias, perineal (Q46406) (← links)
- Congenital chordee (Q46407) (← links)
- Anorchia or microorchidia (Q46408) (← links)
- Hypoplasia of testis or scrotum (Q46409) (← links)
- Polyorchidism (Q46410) (← links)
- Bifid scrotum (Q46411) (← links)
- Agenesis of vas deferens (Q46412) (← links)
- Micropenis or penis agenesis (Q46413) (← links)
- Renal agenesis or other reduction defects of kidney (Q46414) (← links)
- Renal agenesis (Q46415) (← links)
- Autosomal dominant tubulointerstitial disease (Q46416) (← links)
- Congenital single renal cyst (Q46417) (← links)
- Autosomal dominant polycystic kidney disease (Q46418) (← links)
- Renal dysplasia (Q46419) (← links)
- Nephronophthisis (Q46420) (← links)
- Meckel-Gruber syndrome (Q46421) (← links)
- Structural developmental anomalies of urinary tract (Q46422) (← links)
- Duplication of urethra (Q46423) (← links)
- Megacystis-megaureter (Q46424) (← links)
- Congenital megalourethra (Q46425) (← links)
- Congenital hydronephrosis (Q46426) (← links)
