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CLN11 disease
1 OMIM reference -
1 associated gene
37 connected diseases
No signs/symptoms info
Disease Type of connection
Behavioral variant of frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Dyssegmental dysplasia, Silverman-Handmaker type
Schwartz-Jampel syndrome
Intermittent hydrarthrosis
TRAPS syndrome
Tyrosinemia type 2
Heritable pulmonary arterial hypertension
Maternal uniparental disomy of chromosome 14
Paternal uniparental disomy of chromosome 14
Athabaskan brainstem dysgenesis syndrome
Bosley-Salih-Alorainy syndrome
Congenital bilateral absence of vas deferens
Cystic fibrosis
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Male infertility with normal virilization due to meiosis defect
Alternating hemiplegia of childhood
Benign paroxysmal torticollis of infancy
Familial or sporadic hemiplegic migraine
Familial paroxysmal ataxia
Spinocerebellar ataxia type 6
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Acute promyelocytic leukemia
B-cell chronic lymphocytic leukemia
Chuvash erythrocytosis
Dentatorubral pallidoluysian atrophy
Distal 22q11.2 microdeletion syndrome
Gray platelet syndrome
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
Spinocerebellar ataxia type 7
Von Hippel-Lindau disease
Autosomal dominant severe congenital neutropenia
Cyclic neutropenia
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
GRN P28799138945
No signs/symptoms info available.