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 |