Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Neonatal diarrhea |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Perinatal intestinal obstruction (disorder) |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transient neonatal colitis |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal chloridorrhea |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Peptic ulcer of newborn |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Chylous ascites of newborn |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Gastritis of newborn (disorder) |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Newborn ingestion of maternal blood |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Perinatal disorders of liver and/or biliary system |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hematemesis AND/OR melena due to swallowed maternal blood |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Necrotizing enterocolitis in fetus OR newborn (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital fecaliths |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Vomiting in newborn |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Meconium peritonitis |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Perinatal intestinal perforation |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transitory ileus of newborn |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital fecaliths causing obstruction |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Other meconium obstruction |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Other perinatal digestive system disorders |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Other perinatal digestive system disorder NOS |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Perinatal digestive system disorders NOS |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
[X]Digestive system disorders of fetus and newborn |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
[X]Other specified perinatal digestive system disorders |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Meconium obstruction NOS |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Intestinal obstruction by inspissated milk in newborn |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Perinatal intestinal obstruction (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal enamel hypoplasia |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal mass of hypopharynx |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Liver subcapsular hematoma due to birth trauma |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal hepatosplenomegaly |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Perinatal melena |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fetal intrauterine perforation of intestine (disorder) |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal infection of mouth caused by Candida (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal melaena |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal tooth |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Idiopathic transient neonatal hyperinsulinemia (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fetal intrauterine perforation of stomach |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal disorder of oral mucosa |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cholestasis in newborn (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal gastrointestinal disorder |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal hepatocellular damage |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal hepatitis |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transient neonatal hypoglycemia due to hyperinsulinemia (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal haemorrhage of liver |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Neonatal hypotonia of hypopharynx |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Perinatal gastrointestinal hemorrhage |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypoinsulinemic hypoglycaemia and body hemihypertrophy |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fetal gastrointestinal abnormality (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fetal cleft lip (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Injury of liver due to birth trauma (disorder) |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Harlequin fetus |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Progressive familial intrahepatic cholestasis type 2 |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Perinatal necrotizing enterocolitis (disorder) |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Growth delay, intellectual disability, hepatopathy syndrome |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Isolated neonatal sclerosing cholangitis (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Mesenteric pregnancy |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare genetic disease characterized by congenital cataract, neonatal hepatic failure and cholestatic jaundice, and global developmental delay. Neonatal death due to progressive liver failure has been reported. |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pancreatic triacylglycerol lipase deficiency (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pancreatic colipase deficiency |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital anomaly of digestive system |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Mucopolysaccharidosis, MPS-II |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Alstrom syndrome |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Shwachman syndrome |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Intestinal enteropeptidase deficiency |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Periodontal Ehlers-Danlos syndrome |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Peutz-Jeghers syndrome |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Alpha-1-antitrypsin deficiency (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Rotor syndrome (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital secretory diarrhoea |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Intestinal lipofuscinosis |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Glycogen storage disease, hepatic form |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
XTE syndrome |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Persistent tuberculum impar |
Is a |
False |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Crigler-Najjar syndrome, type I (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Glycogen phosphorylase kinase deficiency |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Synthetic defect of bile acids (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Glycogen synthase deficiency |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital pyloric spasm |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital palato-esophageal incoordination |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital functional disorders of the small intestine |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital functional disorders of the colon |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Familial arthrogryposis-cholestatic hepatorenal syndrome |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital viral hepatitis (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital monosaccharide malabsorption |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital atrophy of left lobe of liver |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital disorder of gallbladder and biliary tract |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital achalasia of esophagus |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital velopharyngeal dysfunction |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Omphalocele with obstruction |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hepatomphalocele |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital hiatus hernia |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Oculootodental syndrome |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare, inherited mitochondrial disorder due to a defect in mitochondrial protein synthesis characterized by intrauterine growth retardation, metabolic decompensation with recurrent vomiting, persistent severe lactic acidosis, encephalopathy, seizures, failure to thrive, severe global developmental delay, poor eye contact, severe muscular hypotonia or axial hypotonia with limb hypertonia, hepatomegaly and/or liver dysfunction and/or liver failure, leading to fatal outcome in severe cases. Neuroimaging abnormalities may include corpus callosum thinning, leukodystrophy, delayed myelination and basal ganglia involvement. |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Contiguous ABCD1 DXS1357E deletion syndrome |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital chronic diarrhea with protein-losing enteropathy (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Monostotic fibrous dysplasia of periradicular alveolar bone (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Natal tooth |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Generalized congenital intestinal dysmotility (disorder) |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital chalasia of oesophagus |
Is a |
True |
Disorder of digestive system specific to fetus OR newborn |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|