TESTICULAR PAIN
FOETAL DISORDERS
SCROTAL PAIN
1500
http://purl.bioontology.org/ontology/WHO/1500
V-WHO
LIVEDO RETICULARIS
HYPERTRICHOSIS CONGENITAL
JAW MALFORMATION
CRYPTORCHISM
ENCEPHALOCELE
CHROMOSOME DISORDER
MALFORMATION SKULL
OSTEOCHONDROSIS
DIAPHRAGM APLASIA
FOETAL DISTRESS
NAEVUS
PARALYSIS FLACCID CONGENITAL
MUTAGENIC EFFECT FEMALE
MUTAGENIC EFFECT MALE
BLINDNESS CONGENITAL
URINARY TRACT MALFORMATION
CONGENITAL ANOMALY NOS
DEATH FOETAL
SKIN HYPOPLASIA
MALFORMATION FOOT
PANHYPOPITUITARISM FOETAL
POLYDACTYLY
LIMB MALFORMATION
ABORTION MISSED
ABORTION
PULMONIC STENOSIS CONGENITAL
NYSTAGMUS CONGENITAL
MONGOLISM
MICROCEPHALY
MENINGOMYELOCELE
MALFORMATIONS MULTIPLE
HYPOSPADIAS
HYDROCEPHALUS
JOINT MALFORMATION
HEART MALFORMATION
GI MALFORMATION
OESOPHAGEAL ATRESIA
PATENT DUCTUS ARTERIOSUS
HEARING DISORDER CONGENITAL
ADRENOGENITAL SYNDROME CONGENITAL
EXOMPHALOS
TONGUE TIE
HEMIHYPERTROPHY
TRACHEO-OESOPHAGEAL FISTULA
HERNIA CONGENITAL
RENAL DYSGENESIS
HARELIP
EYE MALFORMATION
ECTROMELIA TWO LIMBS
ECTROMELIA THREE LIMBS
ECTROMELIA ONE LIMB
ECTROMELIA FOUR LIMBS
ECTROMELIA
EAR MALFORMATION
DEAFNESS CONGENITAL
CLUBFOOT
CLEFT PALATE
PULMONARY MALFORMATION
AORTIC STENOSIS
FACE MALFORMATION
PYLORIC STENOSIS
TESTICULAR HYPOPLASIA
GENITAL MALFORMATION
CEREBROVASCULAR DISORDER FOETAL
SKIN MALFORMATION
RENAL AGENESIS
HYDROPS FETALIS
CATARACT CONGENITAL
ANGIOFIBROMA
BRAIN DAMAGE CONGENITAL
ATRIAL SEPTAL DEFECT
ARTERY MALFORMATION
ANOPHTHALMIA
AORTIC COARCTATION
ANUS IMPERFORATE
ANENCEPHALY
MUSCLE MALFORMATION
CHONDRODYSTROPHY
MEGACOLON CONGENITAL
VIRILISM FOETAL
BILIARY ATRESIA
FOETAL MATURATION IMPAIRED
VENTRICULAR SEPTAL DEFECT
HYPOTHYROIDISM CONGENITAL
UROGENITAL MALFORMATION
TRANSPOSITION OF GREAT VESSELS
TOOTH MALFORMATION
SYNDACTYLY
GOITRE CONGENITAL
SPINE MALFORMATION
FOETAL ALCOHOL SYNDROME
SPINA BIFIDA
LIVER AND BILIARY SYSTEM DISORDERS
PHENYLKETONURIA
VASCULAR MALFORMATION CEREBRAL
VASCULAR MALFORMATION PERIPHERAL
ALKAPTONURIA
EPISPADIAS
RESPIRATORY SYSTEM IMMATURE
NEONATAL ADVERSE EFFECT
STILLBIRTH
DWARFISM
MELANOSIS CONGENITAL
RESPIRATORY TRACT MALFORMATION
FOETAL VALPROATE SYNDROME
SEX CHROMOSOME DISORDER
UMBILICAL MALFORMATION
MALFORMATION HAND
PARALYSIS SPASTIC CONGENITAL
NAIL DISORDER CONGENITAL
Sign or Symptom
C0039591