Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Hereditary motor and sensory neuropathy with optic atrophy |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Dominant hereditary optic atrophy |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Leber's optic atrophy |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Hereditary optic atrophy NOS |
Is a |
False |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Early-onset X-linked optic atrophy |
Is a |
False |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Hereditary right optic atrophy |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Hereditary left optic atrophy |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Spastic paraplegia, optic atrophy, neuropathy syndrome |
Is a |
False |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Wolfram-like syndrome |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Infantile cerebellar and retinal degeneration |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Autosomal recessive optic atrophy type 7 |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Fatal X-linked ataxia with deafness and loss of vision |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Autosomal recessive optic atrophy type 6 |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Childhood-onset autosomal dominant optic atrophy |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
X-linked optic atrophy |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome |
Is a |
True |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|
Hereditary optic atrophy NOS |
Is a |
False |
Hereditary optic atrophy |
Inferred relationship |
Existential restriction modifier |
|