Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
syndrome d'Okamoto |
Is a |
False |
Growth retardation (disorder) |
Inferred relationship |
Some |
|
Fallot complex - intellectual deficit - growth delay is a rare disorder characterized by tetralogy of Fallot, minor facial anomalies, and severe intellectual deficiency and growth delay. |
Is a |
True |
Growth retardation (disorder) |
Inferred relationship |
Some |
|
Growth retardation-mild developmental delay-chronic hepatitis syndrome is a rare, genetic, parenchymatous liver disease characterized by pre- and postnatal growth retardation, mild global developmental delay, chronic hepatitis with hepatosplenomegaly, Hashimoto thyroiditis, thrombocytopenia, anemia, and B-precursor acute lymphoblastic leukemia. |
Is a |
True |
Growth retardation (disorder) |
Inferred relationship |
Some |
|
Constitutional delay of growth and puberty |
Is a |
True |
Growth retardation (disorder) |
Inferred relationship |
Some |
|
Root stunting (disorder) |
Is a |
True |
Growth retardation (disorder) |
Inferred relationship |
Some |
|
Nutritional stunting |
Is a |
True |
Growth retardation (disorder) |
Inferred relationship |
Some |
|
Fetal growth retardation (disorder) |
Is a |
True |
Growth retardation (disorder) |
Inferred relationship |
Some |
|
A rare, genetic, syndromic intellectual disability disease characterized by severe intrauterine and post-natal growth delay, moderate to severe intellectual disability, and neonatal-onset hepatopathy with fibrosis, steatosis, and/or cholestasis, occasionally leading to liver failure. Additional variable manifestations include muscular hypotonia, zinc deficiency, recurrent infections, diabetes mellitus, joint contractures, skin and joint laxity, hypervitaminosis D, and sensorineural hearing loss. |
Is a |
True |
Growth retardation (disorder) |
Inferred relationship |
Some |
|