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Fuchs endothelial corneal dystrophy
8 OMIM references -
5 associated genes
55 connected diseases
No signs/symptoms info
Disease Type of connection
Posterior polymorphous corneal dystrophy
Autosomal dominant nonsyndromic intellectual deficit
Congenital hereditary endothelial dystrophy type II
Corneal dystrophy - perceptive deafness
Pallister-Hall syndrome
Pitt-Hopkins syndrome
Primary sclerosing cholangitis
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Precursor T-cell acute lymphoblastic leukemia
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Partial androgen insensitivity syndrome
Catecholaminergic polymorphic ventricular tachycardia
Haddad syndrome
Ondine syndrome
Aneurysm - osteoarthritis syndrome
Familial thoracic aortic aneurysm and aortic dissection
Papillary or follicular thyroid carcinoma
Autosomal recessive primary microcephaly
Hyperparathyroidism - jaw tumor syndrome
Parathyroid carcinoma
Miller-Dieker syndrome
Multiple endocrine neoplasia type 1
Zollinger-Ellison syndrome
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Acute promyelocytic leukemia
Amyotrophic lateral sclerosis
Anophthalmia / microphthalmia - esophageal atresia
Autosomal agammaglobulinemia
Coffin-Siris syndrome
Colobomatous microphthalmia
Familial rhabdoid tumor
Frontotemporal dementia with motor neuron disease
Isolated anophthalmia - microphthalmia
Juvenile amyotrophic lateral sclerosis
Myxofibrosarcoma
Myxoid / round cell liposarcoma
Neuroblastoma
Osteogenesis imperfecta type 3
Precursor B-cell acute lymphoblastic leukemia
Septo-optic dysplasia
Young adult-onset Parkinsonism
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Lethal acantholytic epidermolysis bullosa
Naxos disease
MODY syndrome
Synonym(s):
- Endoepithelial corneal dystrophy
- FECD
- Late hereditary endothelial dystrophy
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: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
8 OMIM references -
No MeSH references
No signs/symptoms info available.