| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Myocardial dysfunction with sepsis |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Myocardial dysfunction with sepsis |
Has interpretation |
True |
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 |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Intellectual disability, expressive aphasia, facial dysmorphism syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Angelman syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Borderline intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Lowe syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Rett's disorder |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Moderate intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Mild intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Seckel syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Cutis laxa-corneal clouding-oligophrenia syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |
| Borjeson-Forssman-Lehmann syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Profound intellectual disability |
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 |
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 |
| Kohlschutter's syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Hennekam syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness |
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 |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| X-linked intellectual disability with marfanoid habitus |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Severe intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Savant syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| MASA syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Blepharophimosis-intellectual disability syndrome, Maat-Kievit-Brunner type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
1 |
| Blepharophimosis-intellectual disability syndrome, SBBYS type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Myhre syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Renpenning syndrome |
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 |
| X-linked intellectual disability-psychosis-macroorchidism syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Partington syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| X-linked intellectual disability Snyder type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Deafness-dystonia-optic neuronopathy syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Lethal ataxia-deafness-optic atrophy |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| CASK related intellectual disability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Neuronal ceroid lipofuscinosis 8 |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Mowat-Wilson syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Autosomal recessive chorioretinopathy and microcephaly syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A (glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A) mutation |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Microcephalic primordial dwarfism Alazami type |
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 |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| 3q27.3 microdeletion syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Microcephaly, thin corpus callosum, intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Optic atrophy, intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Intellectual disability, seizures, macrocephaly, obesity syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |
| Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| 2p13.2 microdeletion syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Developmental delay with autism spectrum disorder and gait instability |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| 5p13 microduplication syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| 11p15.4 microduplication syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Kagami Ogata syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Alopecia, progressive neurological defect, endocrinopathy syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Intellectual disability, short stature, hypertelorism syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Hepatic fibrosis, renal cyst, intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Pseudoleprechaunism syndrome Patterson type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Grubben, De Cock, Borghgraef syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Facial dysmorphism, cleft palate, loose skin syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Craniofaciofrontodigital syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
6 |
| Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Cerebrofacioarticular syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Aortic arch anomaly, facial dysmorphism, intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Wiedemann Steiner syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Intellectual disability due to nutritional deficiency |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Craniodigital syndrome and intellectual disability syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Hypotonia, speech impairment, severe cognitive delay syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Intellectual disability, alacrima, achalasia syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Intellectual disability, polydactyly, uncombable hair syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Intellectual disability, spasticity, ectrodactyly syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
5 |
| Intellectual disability, brachydactyly, Pierre Robin syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Intellectual disability Wolff type |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Macrocephaly and developmental delay syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Malan overgrowth syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
4 |
| Corpus callosum agenesis, abnormal genitalia syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Oro-facial digital syndrome type 14 |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
8 |
| Pachygyria, intellectual disability, epilepsy syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
3 |
| Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
2 |
| Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome |
Has interpretation |
True |
Impaired |
Inferred relationship |
Some |
7 |