| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Congenital hereditary endothelial dystrophy and perceptive deafness syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Oculootoradial syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Mitochondrial myopathy, lactic acidosis, deafness syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Black locks, oculocutaneous albinism, AND deafness of the sensorineural type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
4 |
| Bosley Salih Alorainy syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Caudal appendage deafness syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Cleft palate with coloboma of eye and deafness syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
4 |
| Cleft palate and cleft lip with deafness and sacral lipoma syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Deafness and intellectual disability Martin Probst type syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Congenital cataract with deafness and hypogonadism syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
4 |
| Deafness with cataract and skeletal anomaly syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
4 |
| Deafness with epiphyseal dysplasia and short stature syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
4 |
| Deafness craniofacial syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Deafness with skeletal dysplasia and lip granuloma syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
4 |
| Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Lipodystrophy, intellectual disability, deafness syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Pili torti-deafness syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Spondyloepiphyseal dysplasia with myopia and sensorineural deafness syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
4 |
| X-linked sensorineural hearing loss |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| Combined oxidative phosphorylation defect type 25 |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| Acute kidney injury following administration of contrast media |
Has interpretation |
False |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| Postoperative urinary incontinence |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| Dementia caused by manganese and/or manganese compound |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| Dementia due to thiamine deficiency |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| Dementia due to niacin deficiency |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| Dementia due to nutritional deficiency disorder |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| Dementia due to cobalamin deficiency |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| Dementia due to vitamin E deficiency |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| Cognitive impairment due to lead toxicity |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| Chronic traumatic encephalopathy |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Integral membrane protein 2B related amyloidosis |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Impaired social interaction |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Intellectual disability, epilepsy, extrapyramidal syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
4 |
| Adynamic bone disease |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Impaired renal function disorder |
Has interpretation |
False |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Phosphate-losing tubular disorders |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Renal function impairment with growth failure |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Renal acidemia |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Left ventricular failure with normal ejection fraction due to coronary arteriosclerosis |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Left ventricular failure with normal ejection fraction due to cardiomyopathy |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Left ventricular failure with normal ejection fraction due to myocarditis |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Left ventricular failure with normal ejection fraction due to valvular heart disease |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Myocardial dysfunction with sepsis |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| Myocardial dysfunction with sepsis |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
4 |
| Left ventricular failure with sepsis |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Right ventricular failure with sepsis |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Sanjad Sakati syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
4 |
| Intellectual disability, expressive aphasia, facial dysmorphism syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Angelman syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Borderline intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Lowe syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
4 |
| Rett's disorder |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Moderate intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Mild intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Seckel syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Cutis laxa-corneal clouding-oligophrenia syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
7 |
| Borjeson-Forssman-Lehmann syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Profound intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Hyperphosphatasemia with intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Bardet-Biedl syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Tetrasomy 12p syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Coffin-Siris syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Fragile X syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Kohlschutter's syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
6 |
| Hennekam lymphangiectasia-lymphedema syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
6 |
| Laurence-Moon syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Gillespie syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| X-linked intellectual disability with marfanoid habitus |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Severe intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Savant syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Intellectual disability, aphasia, shuffling gait, adducted thumbs syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
4 |
| Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
1 |
| Blepharophimosis, intellectual disability syndrome, Say-Barber-Biesecker-Young-Simpson type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Myhre syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Renpenning syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Monocarboxylate transporter 8 deficiency |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Pitt-Hopkins syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| X-linked intellectual developmental disorder Christianson type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
4 |
| X-linked intellectual disability-psychosis-macroorchidism syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| X-linked intellectual deficit-dystonia-dysarthria syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| X-linked intellectual disability Snyder type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Deafness-dystonia-optic neuronopathy syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Fatal X-linked ataxia with deafness and loss of vision |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Calcium/calmodulin-dependent serine protein kinase related intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
2 |
| Progressive epilepsy-intellectual disability syndrome Finnish type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Mowat-Wilson syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Autosomal recessive chorioretinopathy and microcephaly syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Early-onset epileptic encephalopathy and intellectual disability due to glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A mutation |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
3 |
| Microcephalic primordial dwarfism Alazami type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| Microcephalic primordial dwarfism Dauber type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |
| X-linked cerebral, cerebellar, coloboma syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
4 |
| Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Existential restriction modifier |
5 |