| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Congenital hereditary endothelial dystrophy and perceptive deafness syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Oculootoradial syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Mitochondrial myopathy, lactic acidosis, deafness syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Black locks, oculocutaneous albinism, AND deafness of the sensorineural type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Bosley Salih Alorainy syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Caudal appendage deafness syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Abruzzo Erickson syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Lowry Yong syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Deafness and intellectual disability Martin Probst type syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Congenital cataract with deafness and hypogonadism syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Deafness with cataract and skeletal anomaly syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Deafness with epiphyseal dysplasia and short stature syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Deafness craniofacial syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Deafness with skeletal dysplasia and lip granuloma syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Lipodystrophy, intellectual disability, deafness syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Björnstad syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Spondyloepiphyseal dysplasia with myopia and sensorineural deafness syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| X-linked sensorineural hearing loss |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Combined oxidative phosphorylation defect type 25 (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Acute kidney injury following administration of contrast media (disorder) |
Has interpretation |
False |
Impaired |
Inferred relationship |
Some |
1 |
| Postoperative urinary incontinence |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Dementia caused by manganese and/or manganese compound (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Dementia due to thiamine deficiency (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Dementia due to niacin deficiency (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Dementia due to nutritional deficiency |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Dementia due to cobalamin deficiency |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Dementia due to vitamin E deficiency (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Cognitive impairment due to lead toxicity (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Chronic traumatic encephalopathy (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Integral membrane protein 2B related amyloidosis (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Impaired social interaction |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Intellectual disability, epilepsy, extrapyramidal syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Adynamic bone disease |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Impaired renal function disorder |
Has interpretation |
False |
Impaired |
Inferred relationship |
Some |
2 |
| Phosphate-losing tubular disorders |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Renal function impairment with growth failure |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Renal acidaemia |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Left ventricular failure with normal ejection fraction due to coronary artery disease |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Left ventricular failure with normal ejection fraction due to cardiomyopathy (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Left ventricular failure with normal ejection fraction due to myocarditis |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Left ventricular failure with normal ejection fraction due to valvular heart disease |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Myocardial dysfunction with sepsis (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Myocardial dysfunction with sepsis (disorder) |
Has interpretation |
False |
Impaired |
Inferred relationship |
Some |
4 |
| Left ventricular failure with sepsis |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Right ventricular failure with sepsis |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Sanjad Sakati syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Intellectual disability, expressive aphasia, facial dysmorphism syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Angelman syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Borderline intellectual disability (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Lowe syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Rett syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Moderate intellectual disability (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Mild intellectual disability (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Seckel syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| de Barsey syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |
| Borjeson-Forssman-Lehmann syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Profound intellectual disability (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Hyperphosphatasaemia with intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Bardet-Biedl syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Tetrasomy 12p syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Coffin-Siris syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Fragile X syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Amelocerebrohypohidrotic syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Hennekam lymphangiectasia-lymphedema syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Laurence-Moon syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Gillespie syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| X-linked intellectual disability with marfanoid habitus (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Severe intellectual disability (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Savant syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| MASA syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Ohdo syndrome, Maat-Kievit-Brunner type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Myhre syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Renpenning syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Allan-Herndon-Dudley syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Pitt-Hopkins syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Christianson syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| PPM-X syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Partington syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Snyder-Robinson syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Deafness-dystonia-optic neuronopathy syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Arts syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Calcium/calmodulin-dependent serine protein kinase related intellectual disability (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Northern epilepsy |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Mowat-Wilson syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Autosomal recessive chorioretinopathy and microcephaly syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A developmental and epileptic encephalopathy (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Microcephalic primordial dwarfism Alazami type (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Microcephalic primordial dwarfism Dauber type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| X-linked cerebral, cerebellar, coloboma syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome (disorder) |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |