| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Paraneoplastic hyponatremia (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Drug-induced hyponatremia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Hyponatremia with extracellular fluid depletion |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Hemolytic uremic syndrome with diacylglycerol kinase epsilon deficiency (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Hemolytic uremic syndrome with diacylglycerol kinase epsilon deficiency (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Hemolytic uremic syndrome with diacylglycerol kinase epsilon deficiency (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
9 |
| Infection-related hemolytic uremic syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Infection-related hemolytic uremic syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Infection-related hemolytic uremic syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Glutathione synthetase deficiency |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Glutathione synthetase deficiency |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Glutathione synthase deficiency without 5-oxoprolinuria |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Glutathione synthase deficiency without 5-oxoprolinuria |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Hyponatremia with decreased serum osmolality |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Microcephaly, facial dysmorphism, ocular anomalies, multiple congenital anomalies syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Density below reference range |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
1 |
| Urine pH below reference range |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
9 |
| Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
10 |
| Postpartum hemolysis-elevated liver enzymes-low platelet count syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Pelvic disproportion due to contracted pelvis |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Fanconi anemia of complementation group C |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Fanconi anemia of complementation group C |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Fanconi anemia of complementation group C |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Fanconi anemia of complementation group C |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| International normalized ratio below reference range (finding) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Ehlers-Danlos and osteogenesis imperfecta syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
6 |
| Spondyloepimetaphyseal dysplasia with joint laxity Beighton type |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Spondyloepimetaphyseal dysplasia with joint laxity exocyst complex component 6B type (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Haemoglobin D beta plus thalassaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Haemoglobin E beta plus thalassaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Haemoglobin C beta plus thalassaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Hemoglobin E beta zero thalassemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Hemoglobin D beta zero thalassemia (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Haemoglobin C beta zero thalassaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Pancytopenia caused by colchicine (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Pancytopenia caused by colchicine (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Pancytopenia caused by colchicine (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Pancytopenia caused by colchicine (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Pancytopenia caused by non-steroidal anti-inflammatory agent (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Pancytopenia caused by non-steroidal anti-inflammatory agent (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Pancytopenia caused by non-steroidal anti-inflammatory agent (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Pancytopenia caused by non-steroidal anti-inflammatory agent (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Delta beta thalassemia trait (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Postpartum iron deficiency anemia (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Postpartum iron deficiency anemia (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Iron deficiency anemia during maternal intrapartum period (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Iron deficiency anemia during maternal intrapartum period (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Glutathione synthase deficiency with 5-oxoprolinuria |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Glutathione synthase deficiency with 5-oxoprolinuria |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Atypical haemolytic uraemic syndrome with complement gene abnormality |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Atypical haemolytic uraemic syndrome with complement gene abnormality |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Atypical haemolytic uraemic syndrome with complement gene abnormality |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
6 |
| Atypical haemolytic uraemic syndrome with anti-factor H antibodies |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Atypical haemolytic uraemic syndrome with anti-factor H antibodies |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Atypical haemolytic uraemic syndrome with anti-factor H antibodies |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
6 |
| Left ventricular pressure during mid-diastole below reference range |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Nocturnal hypoglycaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| SET domain containing 2, histone lysine methyltransferase-related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
6 |
| Congenital pontocerebellar hypoplasia type 11 (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
6 |
| Congenital pontocerebellar hypoplasia type 12 |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
8 |
| Congenital pontocerebellar hypoplasia type 14 |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
6 |
| Periodic fever, immunodeficiency, thrombocytopenia syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Glaucoma, ectopia, microspherophakia, stiff joint, short stature syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
9 |
| AMeD syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| AMeD syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
6 |
| AMeD syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
7 |
| AMeD syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
8 |
| AMeD syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
9 |
| AMeD syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
13 |
| CIMDAG syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
6 |
| Pancytopenia caused by antidiabetic drug (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Pancytopenia caused by antidiabetic drug (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Pancytopenia caused by antidiabetic drug (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Pancytopenia caused by antidiabetic drug (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| TTS (thrombosis with thrombocytopenia syndrome) following non-replicating adenovirus vector COVID-19 vaccination |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| EN1-related dorsoventral syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| EN1-related dorsoventral syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
6 |
| Developmental delay, immunodeficiency, leukoencephalopathy, hypohomocysteinemia syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Dual energy X-ray absorptiometry of neck of femur result osteopenia (finding) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Dual energy X-ray absorptiometry of bone of hip joint region result osteopenia (finding) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Dual energy X-ray absorptiometry of calcaneum result osteoporosis (finding) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Dual energy X-ray absorptiometry of calcaneum result osteopenia (finding) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Dual energy X-ray absorptiometry of bone of forearm result osteopenia (finding) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Dual energy X-ray absorptiometry of bone of forearm result osteoporosis (finding) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Dual energy X-ray absorptiometry of neck of femur result osteoporosis (finding) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Dual energy X-ray absorptiometry of bone of hip joint region result osteoporosis (finding) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Dual energy X-ray absorptiometry of bone of lumbar vertebra result osteoporosis (finding) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Autosomal recessive combined immunodeficiency due to Wiskott Aldrich syndrome protein-interacting protein deficiency (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Autosomal recessive combined immunodeficiency due to Arp2/3-mediated filament branching defect |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Primary hypomagnesaemia, generalised seizures, intellectual disability, obesity syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Thrombosis with thrombocytopenia syndrome following vaccination (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to diaphanous related formin 1 mutation (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Bilateral stiffness of knee joints |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Stiffness of bilateral wrist joints (finding) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Stiffness of bilateral hip joints (finding) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Stiffness of bilateral ankle joints (finding) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |