| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Haemoglobin Paksé disease |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
3 |
| Haemoglobin Paksé disease |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Hemoglobin Seal Rock disease (disorder) |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
3 |
| Hemoglobin Seal Rock disease (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
2 |
| Microcephalus cardiomyopathy syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Microcephalus cleft palate syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Microcephalic primordial dwarfism of Toriello type (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Hadziselimovic syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
6 |
| Microcephalus co-occurrent with cervical spine fusion anomaly (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Microcephalus microcornea syndrome of Seemanova type (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Microcephalus with albinism and digital anomaly syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
7 |
| Microcephalus with brachydactyly and kyphoscoliosis syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
6 |
| Microcephalus with cardiac defect and lung malsegmentation syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Drug-induced non autoimmune haemolytic anaemia |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
4 |
| Drug-induced non autoimmune haemolytic anaemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Iron deficiency anaemia due to coeliac disease |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Iron deficiency anaemia due to coeliac disease |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Iron deficiency anemia due to increased requirement in adolescence (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Iron deficiency anemia due to increased requirement in adolescence (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Acquired iron deficiency anaemia due to increased requirement in infancy |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Acquired iron deficiency anaemia due to increased requirement in infancy |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Iron deficiency anemia following gastrectomy (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Iron deficiency anemia following gastrectomy (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Microcephalus, brain defect, spasticity, hypernatremia syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Microcephalus, complex motor and sensory axonal neuropathy syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
6 |
| Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Microcephalus, glomerulonephritis, marfanoid habitus syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Microcephaly with deafness and intellectual disability syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Microcephalus, lymphedema, chorioretinopathy syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Microcephaly with simplified gyral pattern |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Microcephaly, seizure, intellectual disability, heart disease syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Microcephaly-capillary malformation syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Microcephaly, thin corpus callosum, intellectual disability syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Felty's syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Neu-Laxova syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Nijmegen breakage syndrome-like disorder (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Oculocerebrofacial syndrome Kaufman type (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Oro-facial digital syndrome type 14 |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
7 |
| Oculopalatocerebral syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Prominent glabella with microcephaly and hypogenitalism syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Seckel syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Radioulnar synostosis with microcephaly and scoliosis syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
6 |
| Pseudoprogeria syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Severe neonatal onset encephalopathy with microcephaly (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Severe X-linked intellectual disability Gustavson type (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Child HC < 0.4th centile |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Child HC = 0.4th centile |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Child HC 0.5th - 1.9th centile |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Child HC = 2nd centile |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Nijmegen breakage syndrome-like disorder (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Microcephalic primordial dwarfism of Toriello type (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Microcephalic primordial dwarfism Alazami type (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Microcephalic primordial dwarfism Dauber type |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Hadziselimovic syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Cleft palate, large ears, small head syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Epiphyseal dysplasia, microcephalus, nystagmus syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Cutaneous mastocytosis, short stature, hearing loss syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
8 |
| Microcephalic osteodysplastic primordial dwarfism types I and III (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Seckel syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Microcephalic osteodysplastic dysplasia Saul Wilson type (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Stimmler syndrome |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
7 |
| Microcephalus with brachydactyly and kyphoscoliosis syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Microcephalic primordial dwarfism Montreal type |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Radioulnar synostosis with microcephaly and scoliosis syndrome (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Fecal lipase below reference range |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Feces pH more acidic than reference range (finding) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Anemia caused by antineoplastic agent |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Anemia caused by antineoplastic agent |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Pancytopenia caused by anticonvulsant |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Pancytopenia caused by anticonvulsant |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Pancytopenia caused by anticonvulsant |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Pancytopenia caused by anticonvulsant |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Pancytopenia caused by antithyroid drug (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Pancytopenia caused by antithyroid drug (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
5 |
| Pancytopenia caused by antithyroid drug (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Pancytopenia caused by antithyroid drug (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
4 |
| Anemia due to enzymopathy (disorder) |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
1 |
| Anemia due to enzymopathy (disorder) |
Has interpretation |
False |
Below reference range |
Inferred relationship |
Some |
2 |
| Homozygous hereditary elliptocytosis (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Homozygous hereditary elliptocytosis (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |
| Hereditary iron deficiency anemia |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
1 |
| Vitamin B12 deficiency anemia due to chronic atrophic gastritis (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
3 |
| Vitamin B12 deficiency anemia due to chronic atrophic gastritis (disorder) |
Has interpretation |
True |
Below reference range |
Inferred relationship |
Some |
2 |