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Congenital stationary night blindness
11 OMIM references -
14 associated genes
31 connected diseases
No signs/symptoms info
Disease Type of connection
Retinitis pigmentosa
Oguchi disease
Cone rod dystrophy
Retinitis punctata albescens
Ã…land Islands eye disease
Precursor T-cell acute lymphoblastic leukemia
Berardinelli-Seip congenital lipodystrophy
Diffuse cutaneous systemic sclerosis
Heritable pulmonary arterial hypertension
Limited cutaneous systemic sclerosis
Idiopathic CD4 lymphocytopenia
Joubert syndrome with orofaciodigital defect
Parkinsonian-pyramidal syndrome
Young adult-onset Parkinsonism
Young adult-onset distal hereditary motor neuropathy
Adult-onset distal myopathy due to VCP mutation
Amyotrophic lateral sclerosis
Autosomal agammaglobulinemia
Behavioral variant of frontotemporal dementia
Burkitt lymphoma
Chronic myeloid leukemia
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Precursor B-cell acute lymphoblastic leukemia
Progressive non-fluent aphasia
SHORT syndrome
Semantic dementia
Spastic paraplegia - Paget disease of bone
X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Bradyopsia
Catecholaminergic polymorphic ventricular tachycardia
Early infantile epileptic encephalopathy
Synonym(s):
- Congenital essential nyctalopia
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
11 OMIM references -
1 MeSH reference: C536122
No signs/symptoms info available.