A	C124224	Pigmentary Change in Skin	Pigmentary Change of Skin		Abnormal skin pigmentation.	Changes in skin pigmentation.	C36281	Integumentary System Finding			C90259	Pediatric Terminology		
A	C3568	Malignant Brain Neoplasm	Malignant Brain Tumor		A primary or metastatic malignant neoplasm affecting the brain.	An abnormal solid mass arising within the brain with histologic features suggesting the potential to metastasize.	C9305	Cancer			C90259	Pediatric Terminology		
C	C123202	Oligomeganephronia	Oligomeganephronia		Congenital renal hypoplasia characterized by small kidneys; reduced nephron number; tubular and glomerular hypertrophy.	Congenital renal hypoplasia characterized by small kidneys; reduced nephron number; tubular and glomerular hypertrophy.	C34843	Nephropathy			C90259	Pediatric Terminology		
C	C123185	P3 Hydronephrosis	P3 Hydronephrosis		Postnatal Hydronephrosis with the following clinical findings: 1) calyceal dilation and the ureter are the same as those in UTD P2, 2) the renal parenchymal is thinned, has increased echogenicity and/or has decreased corticomedullary differentiation, or 3) the bladder is abnormal (wall thickening, ureterocele, posterior urethral dilation). Cases in which there are parenchymal abnormalities but the APRPD is less than 15 mm, are classified as UTD P3. (Adapted from: Hiep T. Nguyen, Carol B. Benson, Bryann Bromley, Jeffrey B. Campbell, Jeanne Chow, Beverly Coleman, Christopher Cooper, Jude Crino, Kassa Darge, C.D. Anthony Herndon, Anthony O. Odibo, Michael J.G. Somers, Deborah R. Stein; Multidisciplinary consensus on the classification of prenatal and postnatal urinary tract dilation (UTD classification system); Pediatric Urology; December 2014 Volume 10, Issue 6, Pages 982-998)	Postnatal Hydronephrosis with the following clinical findings: 1) calyceal dilation and the ureter are the same as those in UTD P2, 2) the renal parenchymal is thinned, has increased echogenicity and/or has decreased corticomedullary differentiation, or 3) the bladder is abnormal (wall thickening, ureterocele, posterior urethral dilation). Cases in which there are parenchymal abnormalities but the APRPD is less than 15 mm, are classified as UTD P3. (Adapted from: Hiep T. Nguyen, Carol B. Benson, Bryann Bromley, Jeffrey B. Campbell, Jeanne Chow, Beverly Coleman, Christopher Cooper, Jude Crino, Kassa Darge, C.D. Anthony Herndon, Anthony O. Odibo, Michael J.G. Somers, Deborah R. Stein; Multidisciplinary consensus on the classification of prenatal and postnatal urinary tract dilation (UTD classification system); Pediatric Urology; December 2014 Volume 10, Issue 6, Pages 982-998)	C26796	Hydronephrosis			C90259	Pediatric Terminology		
C	C84473	Atrial Septal Defect	Atrial Septal Defect		The presence of a defect (opening) in the septum that separates the two atria of the heart. It can be congenital or acquired.		C84482	Congenital Septal Defect			C90259	Pediatric Terminology		
C	C113743	Excessive Bruising	Excessive Bruising		Bruising that is disproportionately high to the amount of trauma received or reported.	Bruising that is disproportionally high for the associated trauma.	C100104	Sign or Symptom			C90259	Pediatric Terminology		
C	C117246	Decreased Concentration	Decreased Concentration		Reduced ability to sustain attention.	Impaired ability to sustain attention.	C3858	Mental and Behavioral Signs and Symptoms			C90259	Pediatric Terminology		
C	C118676	Perinatal Mortality	Perinatal Mortality		Fetal or infant death during the period of time that includes the antepartum, intrapartum, and neonatal stages.	Fetal or infant death during the period of time that includes the antepartum, Intrapartum, and neonatal stages.	C90491	Pregnancy Outcome			C90259	Pediatric Terminology		
C	C3408	Thrombocytopenia	Thrombocytopenia	Thrombocytopenic Disorder	A laboratory test result indicating that there is an abnormally small number of platelets in the circulating blood.	Abnormally low level of platelets in the blood.	C26323	Hematologic Disorder	C36292	Laboratory Test Result	C90259	Pediatric Terminology		
D	C117250	Hypomanic Mood	Hypomanic Mood		An emotional state characterized by mild to moderate elevation of mood without relevant effect of functioning.	An emotional state characterized by mild to moderate elevation of mood without relevant effect on functioning.	C3858	Mental and Behavioral Signs and Symptoms			C90259	Pediatric Terminology		
D	C118762	Enopthalmos	Enopthalmos		The posterior displacement of the eye within the orbit.	The posterior displacement of the eye within the orbit.	C99208	Eye Finding			C90259	Pediatric Terminology		
D	C123224	Branchio-oto-renal Syndrome	Branchio-oto-renal Syndrome	Branchiootorenal Syndrome	A hereditary disorder caused by mutations in the EYA1 gene, which is characterized by hearing loss, structural defects of the ear, branchial fistulas or cysts, and early, progressive chronic renal failure.	A hereditary disorder caused by mutations in the EYA1 gene, which is characterized by hearing loss, structural defects of the ear, branchial fistulas or cysts, and early, progressive chronic renal failure.	C28193	Syndrome			C90259	Pediatric Terminology		
D	C3327	Skin Discoloration	Pigmentary Change of Skin	Dyschromia	Abnormal changes in skin coloration.	Abnormal changes in skin coloration.	C36281	Integumentary System Finding			C90259	Pediatric Terminology		
D	C43262	Exophthalmos	Exophthalmos		A protrusion of the eyeball from the socket.		C99208	Eye Finding			C90259	Pediatric Terminology