| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Benign scapuloperoneal muscular dystrophy |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Severe scapuloperoneal muscular dystrophy with cardiomyopathy |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Robinow syndrome |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
5 |
| Benign congenital muscular dystrophy with finger flexion contractures |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Distal muscular dystrophy |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Larsen-like syndrome beta-1,3-glucuronyltransferase 3 type |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
6 |
| Autosomal recessive limb girdle muscular dystrophy type 2Y |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Hip dysplasia Beukes type |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Congenital muscular dystrophy without intellectual disability |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital muscular dystrophy with cerebellar involvement |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Autosomal recessive limb girdle muscular dystrophy type 2C |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal recessive limb girdle muscular dystrophy type 2F |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Cranio-cervical dystonia with laryngeal and upper limb involvement |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
1 |
| Transient infantile osteopetrosis |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Autosomal dominant limb girdle muscular dystrophy type 1B |
Clinical course |
False |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Leri-Weill dyschondrosteosis |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal recessive limb girdle muscular dystrophy type 2B |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal recessive limb girdle muscular dystrophy type 2I |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Non-Alzheimer's progressive dysphasia |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Progressive aphasia in Alzheimer's disease |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
4 |
| Semantic dementia |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Myopic macular degeneration of bilateral eyes |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Myopic macular degeneration of right eye |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Myopic macular degeneration of left eye |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Progressive aphasia |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Essential iris atrophy |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Progressive cone dystrophy (without rod involvement) |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Multiple progressive hemangiomata |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Secondary pigmentary retinal degeneration |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Degenerative progressive high myopia |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Myopic macular degeneration |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Degenerative progressive high myopia of right eye |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Degenerative progressive high myopia of left eye |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Degenerative progressive high myopia of bilateral eyes |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Post poliomyelitis syndrome |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Progression of fetal right ventricular outflow tract obstruction |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Progression of fetal left ventricular outflow tract obstruction |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| North American Indian childhood cirrhosis |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
4 |
| Progressive external ophthalmoplegia |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Autosomal recessive spastic paraplegia type 55 |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
4 |
| Autosomal recessive spastic paraplegia type 57 |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
4 |
| Spastic paraplegia, optic atrophy, neuropathy syndrome |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
4 |
| Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Primary progressive non fluent aphasia |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Logopenic progressive aphasia |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
5 |
| Mitochondrial neurogastrointestinal encephalomyopathy syndrome |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
5 |
| Progressive external ophthalmoplegia, myopathy, emaciation syndrome |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
5 |
| Alexander's disease |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
4 |
| ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
4 |
| Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
4 |
| Progressive cone-rod dystrophy |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Progressive muscular atrophy |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Progressive multiple sclerosis |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
1 |
| Secondary progressive multiple sclerosis |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Primary progressive multiple sclerosis |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Progressive relapsing multiple sclerosis |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Progressive focal cortical atrophy |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
1 |
| Benign monomelic amyotrophy |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Autosomal dominant progressive external ophthalmoplegia |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive progressive external ophthalmoplegia |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
1 |
| X-linked progressive cerebellar ataxia |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
1 |
| Progressive deafness with stapes fixation |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary cerebral amyloid angiopathy, Dutch type |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
1 |
| Hereditary cerebral hemorrhage with amyloidosis |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary cerebral amyloid angiopathy, Icelandic type |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Progressive pigmentary dermatosis of Schamberg |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Amyotrophic lateral sclerosis, parkinsonism, dementia complex |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Keratosis lichenoides chronica |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Progressive epilepsy-intellectual disability syndrome Finnish type |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Van Bogaert's sclerosing leukoencephalitis |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
4 |
| Granulomatosis disciformis et progressiva |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Chronic progressive coccidioidal pneumonia |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Rett's disorder |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Cirrhosis of liver due to and following cardiac procedure |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
4 |
| Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Progressive external ophthalmoplegia of bilateral eyes |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
1 |
| Progressive cribriform and zosteriform hyperpigmentation |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Progressive peripheral pterygium of right eye |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Progressive peripheral pterygium of left eye |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Progressive peripheral pterygium of bilateral eyes |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
5 |
| Peripheral pterygium, progressive |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Necrobiotic xanthogranuloma |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Necrobiotic xanthogranuloma with paraproteinemia |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Autosomal dominant Robinow syndrome |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive Robinow syndrome |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Bilateral Madelung deformity |
Clinical course |
False |
Progressive |
Inferred relationship |
Existential restriction modifier |
7 |
| Congenital muscular dystrophy type 1D large gene mutation |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Progressive avascular necrosis of bilateral lunate bones |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Cirrhosis of liver due to classical cystic fibrosis |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Autosomal dominant Emery-Dreifuss muscular dystrophy |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Mesomelic dysplasia of upper limb |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Progressive nodular fibrosis of skin |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Porokeratosis of Mibelli |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Giant porokeratosis |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
3 |
| Congenital cataract with ataxia and deafness syndrome |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
4 |
| Chronic progressive epilepsia partialis continua of childhood |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
2 |
| Chronic progressive epilepsia partialis continua |
Clinical course |
True |
Progressive |
Inferred relationship |
Existential restriction modifier |
1 |