| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Sorsby pseudoinflammatory fundus dystrophy (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Lipoid dermatoarthritis |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
4 |
| Spastic ataxia, dysarthria due to glutaminase deficiency (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Progressive shortening of uterine cervix |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Alexander disease juvenile form |
Clinical course |
False |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Alexander disease type I (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Alexander disease adult form |
Clinical course |
False |
Progressive (qualifier value) |
Inferred relationship |
Some |
4 |
| Autosomal dominant complex hereditary spastic paraplegia (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
5 |
| Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
6 |
| Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
5 |
| Epiphyseal, vertebral, ear dysplasia, nose plus associated findings syndrome (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
5 |
| Familial gigantiform cementoma of jaw (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Adult vitelliform macular dystrophy |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Best vitelliform macular dystrophy (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Benign monomelic amyotrophy of lower limb (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Benign monomelic amyotrophy of upper limb (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Autosomal dominant osteopetrosis type 1 |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Birnbaum's syndrome |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
5 |
| Fish-eye disease |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Chronic progressive non-hereditary chorea |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
1 |
| Progressive internal resorption of tooth caused by bacteria (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Friedreich ataxia |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Spinocerebellar ataxia type 46 (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Spinocerebellar ataxia type 45 (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Laminin alpha-2 related limb girdle muscular dystrophy R23 (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Protein O-mannose beta-1,4-n-acetylglucosaminyltransferase 2-related limb girdle muscular dystrophy R24 (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Calpain-3-related limb girdle muscular dystrophy D4 |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Multiple mitochondrial dysfunctions syndrome type 5 (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
4 |
| Multiple mitochondrial dysfunctions syndrome type 6 (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Hemifacial spasm |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Clonic hemifacial spasm |
Clinical course |
False |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Hemifacial spasm of right facial nerve |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Hemifacial spasm of left facial nerve |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Bilateral hemifacial spasm |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
5 |
| Dystonia 28 |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
1 |
| Spondyloepimetaphyseal dysplasia with joint laxity Beighton type |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
5 |
| Spondyloepimetaphyseal dysplasia with joint laxity exocyst complex component 6B type (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
6 |
| Progressive familial intrahepatic cholestasis type 4 (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
1 |
| Neurogenic muscle weakness, ataxia and retinitis pigmentosa (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Essential iris atrophy of bilateral eyes (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
5 |
| Essential iris atrophy of right eye (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Essential iris atrophy of left eye (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Sorsby pseudoinflammatory fundus dystrophy of right eye (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Sorsby pseudoinflammatory fundus dystrophy of left eye (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Sorsby pseudoinflammatory fundus dystrophy of bilateral eyes (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| O'Sullivan McLeod syndrome |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Adult-onset progressive leukoencephalopathy, early-onset deafness (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Congenital pontocerebellar hypoplasia type 14 |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
7 |
| Mitchell syndrome |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| IRF2BPL-related regressive neurodevelopmental disorder, dystonia, seizures syndrome |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Pumilio RNA binding family member 1-related cerebellar ataxia (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
4 |
| Microphthalmia with brain atrophy syndrome (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
6 |
| Acquired progressive esotropia due to high myopia (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
11 |
| Alexander disease type II |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
4 |
| Corticobasal degeneration |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
4 |
| Juvenile Parkinson's disease |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Orthostatic hypotension co-occurrent and due to Parkinson's disease (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
1 |
| Atypical Parkinsonism (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Sporadic Parkinson disease (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Atypical juvenile parkinsonism (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Young onset Parkinson disease (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Early onset parkinsonism and intellectual disability syndrome (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
6 |
| Autosomal dominant late onset Parkinson disease (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Multiple system atrophy, Parkinson variant (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Parkinson's disease |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Psychosis co-occurrent and due to Parkinson's disease (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
4 |
| Autosomal recessive familial Parkinson disease |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Off-periods in Parkinson disease not responding to oral treatment |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Werdnig-Hoffmann disease |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Adult spinal muscular atrophy |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Kugelberg-Welander disease |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Spinal muscular atrophy |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Spinal muscular atrophy, type II |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Progressive bulbar palsy of childhood |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Distal spinal muscular atrophy |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Scapuloperoneal spinal muscular atrophy |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Facioscapulohumeral spinal muscular atrophy |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Facioscapulohumeral spinal muscular atrophy with sensory loss |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Scapulohumeral spinal muscular atrophy |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Oculopharyngeal spinal muscular atrophy |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Bulbospinal neuronopathy |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Spinal muscular atrophy with progressive myoclonic epilepsy (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Spinal muscular atrophy with respiratory distress type 2 |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
4 |
| Spinal atrophy, ophthalmoplegia, pyramidal syndrome |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
5 |
| Autosomal dominant congenital benign spinal muscular atrophy |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| X-linked distal spinal muscular atrophy type 3 (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
3 |
| Autosomal dominant childhood-onset proximal spinal muscular atrophy (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| X-linked distal arthrogryposis multiplex congenita (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
5 |
| Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
6 |
| Chloride voltage-gated channel 6-related childhood-onset progressive neurodegeneration, peripheral neuropathy syndrome (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Progressive external ophthalmoplegia of left eye (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
1 |
| Right progressive external ophthalmoplegia |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
1 |
| Posterior cord syndrome due to Friedreich ataxia (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Fibrosis, neurodegeneration, cerebral angiomatosis syndrome |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
4 |
| Intermediate collagen VI-related muscular dystrophy (disorder) |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
2 |
| Concato's disease |
Clinical course |
True |
Progressive (qualifier value) |
Inferred relationship |
Some |
4 |