| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 5 | 
| Decreased placental secretion of chorionic gonadotropin | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Urine 17 ketogenic steroid below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| High density lipoprotein below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Low density lipoprotein cholesterol below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Cholesterol/high density lipoprotein ratio below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Microcephaly, congenital cataract, psoriasiform dermatitis syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Hereditary thrombocytopenia with early-onset myelofibrosis | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 2 | 
| Euglobulin clot lysis time below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 2 | 
| Serum total protein below reference level | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| X-linked intellectual developmental disorder Christianson type | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 2 | 
| Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Congenital generalized hypercontractile muscle stiffness syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 2 | 
| Oral-facial-digital syndrome with short stature and brachymesophalangia | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 5 | 
| Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Blood magnesium below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Blood glucose below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Blood urea below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Respiratory flow rate below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Decreased forced expiratory volume | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Forced expiratory volume in one second/Forced vital capacity less than 70 percent of predicted | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Forced expiratory volume in one second/Forced vital capacity greater than 70 percent of predicted | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Forced vital capacity below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Lung function mildly obstructed | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Lung function significantly obstructed | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Chest expansion reduced | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Decreased functional residual capacity | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Decreased total lung capacity | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Decreased lung compliance | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Low ventilation-perfusion ratio | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Decreased diffusion capacity of lung | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Blood viscosity below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Familial steroid-resistant nephrotic syndrome with adrenal insufficiency | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 2 | 
| Basal metabolic rate below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Slow metabolic rate | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Urine calcium below reference level | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Urine urate below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Serum chloride below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Serum copper below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Arterial oxygen concentration below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Arterial partial pressure of carbon dioxide below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Microcephalic cortical malformations, short stature due to rotatin deficiency | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Microcephalic cortical malformations, short stature due to rotatin deficiency | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Decreased maximal voluntary ventilation | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Autosomal dominant thrombocytopenia with platelet secretion defect | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Serum calcium below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Short stature, brachydactyly, obesity, global developmental delay syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Severe autosomal recessive macrothrombocytopenia | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 2 | 
| Congenital ichthyosis, microcephalus, tetraplegia syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Sanjad Sakati syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Combined immunodeficiency, enteropathy spectrum | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinemia | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 2 | 
| Short stature, advanced bone age, early-onset osteoarthritis syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 2 | 
| X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Bilateral hip and radial head dislocations, short stature, scoliosis, carpal coalition, pes cavus, facial dysmorphism syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 8 | 
| Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Microcephalic osteodysplastic primordial dwarfism type II | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Microcephalic osteodysplastic primordial dwarfism type II | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Progressive cerebello-cerebral atrophy | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Congenital autosomal recessive small-platelet thrombocytopenia | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 5 | 
| Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Stiffness of joint of bilateral foot regions | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| L-ferritin deficiency | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Hyperostosis cranialis interna | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Phospholipase A2 activating protein-associated neurodevelopmental disorder | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| Severe myopia, generalized joint laxity, short stature syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Glutamine rich 1-related intellectual disability, chondrodysplasia syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 8 | 
| Microcephalic primordial dwarfism, insulin resistance syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 2 | 
| Microcephalic primordial dwarfism, insulin resistance syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Ring finger protein 13-related severe early-onset epileptic encephalopathy | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 2 | 
| 1p35.2 microdeletion syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Complex lethal osteochondrodysplasia | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 2 | 
| Amniotic fluid volume below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 1 | 
| 9q33.3q34.11 microdeletion syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| 11q22.2q22.3 microdeletion syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| 19p13.3 microduplication syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Hemoglobin E/beta thalassemia disease | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 2 | 
| Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| DNA replication fork stabilization factor DONSON-related microcephaly, short stature, limb abnormalities spectrum | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| DNA replication fork stabilization factor DONSON-related microcephaly, short stature, limb abnormalities spectrum | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Placental volume below reference range | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 2 | 
| Lethal fetal cerebrorenogenitourinary agenesis or hypoplasia syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| 46,XX ovarian dysgenesis, short stature syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 3 | 
| Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leukoencephalopathy | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 4 | 
| nudE neurodevelopment protein 1-related microhydranencephaly | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 5 | 
| Cerebellar-facial-dental syndrome | Has interpretation | True | Below reference range | Inferred relationship | Existential restriction modifier | 5 |