Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Asymmetrical growth retardation |
Associated morphology |
False |
Growth retardation |
Inferred relationship |
Some |
1 |
Symmetrical growth retardation |
Associated morphology |
False |
Growth retardation |
Inferred relationship |
Some |
1 |
Fetal growth retardation (disorder) |
Associated morphology |
False |
Growth retardation |
Inferred relationship |
Some |
1 |
Fetal growth retardation NOS |
Associated morphology |
False |
Growth retardation |
Inferred relationship |
Some |
1 |
Symmetrical growth retardation |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
1 |
Asymmetrical growth retardation |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
1 |
Fetal growth retardation NOS |
Associated morphology |
False |
Growth retardation |
Inferred relationship |
Some |
1 |
Fetal growth retardation (disorder) |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
1 |
Fetal growth retardation, antenatal |
Associated morphology |
False |
Growth retardation |
Inferred relationship |
Some |
2 |
Constitutional delay of growth and puberty |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
1 |
Physical retardation due to protein-calorie malnutrition |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
2 |
Nutritional stunting |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
2 |
Arrested development following protein-calorie malnutrition |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
3 |
Moderate nutritional stunting in infancy childhood and adolescence |
Associated morphology |
False |
Growth retardation |
Inferred relationship |
Some |
3 |
Severe nutritional stunting in infancy childhood and adolescence |
Associated morphology |
False |
Growth retardation |
Inferred relationship |
Some |
3 |
Nutritional stunting in infancy (disorder) |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
3 |
Nutritional stunting in childhood (disorder) |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
3 |
Nutritional stunting in adolescence (disorder) |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
3 |
Root stunting (disorder) |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
1 |
Asymmetrical small for gestational age fetus (disorder) |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
1 |
Symmetrical small for gestational age fetus (disorder) |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
1 |
Light-for-dates with signs of fetal malnutrition |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
3 |
Light-for-dates without fetal malnutrition |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
1 |
Small for gestational age fetus |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
1 |
Fetus small-for-dates with signs of malnutrition |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
1 |
Growth retardation (disorder) |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
1 |
syndrome d'Okamoto |
Associated morphology |
False |
Growth retardation |
Inferred relationship |
Some |
5 |
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. |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
5 |
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. |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
3 |
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. |
Associated morphology |
True |
Growth retardation |
Inferred relationship |
Some |
1 |