C	C3718	Wilms Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation Syndrome	11p Partial Monosomy Syndrome		A very rare congenital condition involving the complex of Wilms tumor, aniridia, genitourinary abnormalities, and mental retardation. Wilms Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation (WAGR) syndrome involves deletions of several adjacent genes in chromosome region 11p13. Two or more of the four conditions must be present for an individual to be diagnosed with WAGR Syndrome. The clinical picture varies, depending upon the combination of abnormalities.		C2950	Chromosomal Abnormality			C99147	Neonatal Research Network Terminology		
C	C78603	Scoliosis	Scoliosis		A congenital or acquired spinal deformity characterized by lateral curvature of the spine.		C107377	Musculoskeletal System Disorder	C99064	Spinal Deformity	C99147	Neonatal Research Network Terminology		
C	C85874	Microcephaly	Microcephaly	Microcephalus	A congenital or acquired developmental disorder in which the circumference of the head is smaller than normal for the person's age and sex.		C96412	Brain Development Abnormality			C99147	Neonatal Research Network Terminology		
C	C101270	Kernicterus Related to Isoimmunization	Kernicterus related to Isoimmunization	Kernicterus due to Isoimmunization	Encephalopathy in infants due to high levels of unconjugated bilirubin that are a result of Rh incompatibility between the mother and the fetus.		C26920	Encephalopathy			C99147	Neonatal Research Network Terminology		
C	C101272	Spinal Cord Infarct During Birth	Spinal Cord Infarct during Birth		Ischemic necrosis of the spinal cord due to spinal artery occlusion during the birthing process.		C101035	Birth Injury|Neonatal Injury Related to Birth			C99147	Neonatal Research Network Terminology		
C	C103919	Solitary Multilocular Kidney Cyst	Solitary Multilocular Renal Cyst		A single cyst in the kidney with several compartments.		C2978	Cyst	C3149	Kidney Disease	C99147	Neonatal Research Network Terminology		
C	C3149	Kidney Disorder	Kidney Disease		A neoplastic or non-neoplastic condition affecting the kidney. Representative examples of non-neoplastic conditions include glomerulonephritis and nephrotic syndrome. Representative examples of neoplastic conditions include benign processes (e.g., renal lipoma and renal fibroma) and malignant processes (e.g., renal cell carcinoma and renal lymphoma).		C3430	Urinary System Disorder			C99147	Neonatal Research Network Terminology		
C	C40407	Kidney Wilms Tumor	Nephroblastoma		An embryonal pediatric tumor of the kidney which may also be seen rarely in adults. The peak incidence of Wilms tumor is between the second and fifth year of life. Microscopically, it is composed of a mixture of cellular elements (blastemal, stromal, and epithelial). The most common sites of metastasis include the regional lymph nodes, lungs, and liver.		C9305	Cancer|Malignant Neoplasm			C99147	Neonatal Research Network Terminology		
D	C110943	Musculoskeletal Injury	Injury of Musculoskeletal System		Damage to the muscles, bones and their supportive structral attachments.		C3671	Injury			C99147	Neonatal Research Network Terminology		
D	C117115	Fatty Acid Metabolism Disorder	Fatty Acid Metabolism Disorder	Disorder of Fatty Acid Metabolism	A group of genetic disorders that result from the inability to produce or use an enzyme required to oxidize fatty acids, resulting in an inability to generate energy from fatty acid sources.		C97092	Lipid Metabolism Disorder			C99147	Neonatal Research Network Terminology		
D	C77140	Clinical Test Result	Clinical Test Result	Evaluation Finding	The result of a laboratory, radiologic, or other clinical test performed to determine the presence, absence, or degree of a condition.		C70856	Observational Result			C99147	Neonatal Research Network Terminology		
D	C84509	Primary Malignant Neoplasm	Primary Malignant Neoplasm		A malignant tumor at the original site of growth.		C9305	Cancer|Malignant Neoplasm			C99147	Neonatal Research Network Terminology		
D	C85866	Autosomal Recessive Disorder	Autosomal Recessive Disorder	Autosomal Recessive Hereditary Disorder	An inherited disorder manifested only when two copies of a mutated gene are present.		C3101	Genetic Disorder			C99147	Neonatal Research Network Terminology		
D	C98643	Venous Stenosis	Venous Stenosis		A finding indicating narrowing of a vein in one or multiple areas.		C35117	Vascular Disorder			C99147	Neonatal Research Network Terminology		
D	C98829	Autosomal Dominant Disorder	Autosomal Dominant Disorder	Autosomal Dominant Hereditary Disorder	An inherited disorder that manifests when one copy of a mutated gene is present.		C3101	Genetic Disorder			C99147	Neonatal Research Network Terminology		
D	C99062	Skin Injury	Skin Injury	Injury of Integument	Damage to the skin.		C3671	Injury			C99147	Neonatal Research Network Terminology