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Nuclear cataract
13 OMIM references -
10 associated genes
76 connected diseases
No signs/symptoms info
Disease Type of connection
Cataract-microcornea syndrome
Zonular cataract
Coppock-like cataract
Cerulean cataract
Total congenital cataract
Cataract with Y-shaped suture opacities
Pulverulent cataract
Posterior polar cataract
Coralliform cataract
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Nance-Horan syndrome
Wolfram syndrome
Familial isolated dilated cardiomyopathy
Alpha-crystallinopathy
Fatal infantile hypertonic myofibrillar myopathy
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Distal hereditary motor neuropathy type 2
Microphthalmia - cataract
Congenital bilateral absence of vas deferens
Cystic fibrosis
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Male infertility with normal virilization due to meiosis defect
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Craniometaphyseal dysplasia
Hypoplastic left heart syndrome
Oculodentodigital dysplasia
Syndactyly type 3
Atypical Werner syndrome
Autosomal codominant severe lipodystrophic laminopathy
Autosomal dominant Emery-Dreifuss muscular dystrophy
Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal recessive Emery-Dreifuss muscular dystrophy
Charcot-Marie-Tooth disease type 2B1
Congenital dyserythropoietic anemia type II
Congenital muscular dystrophy due to LMNA mutation
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Familial partial lipodystrophy, Dunnigan type
Familial partial lipodystrophy, Köbberling type
Heart-hand syndrome, Slovenian type
Hutchinson-Gilford progeria syndrome
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Leber congenital amaurosis
Left ventricular noncompaction
Lethal restrictive dermopathy
Mandibuloacral dysplasia with type A lipodystrophy
Progeria-associated arthropathy
Senior-Loken syndrome
X-linked Emery-Dreifuss muscular dystrophy
Catecholaminergic polymorphic ventricular tachycardia
Congenital dyserythropoietic anemia type III
Papillary or follicular thyroid carcinoma
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Berardinelli-Seip congenital lipodystrophy
Diffuse cutaneous systemic sclerosis
Heritable pulmonary arterial hypertension
Limited cutaneous systemic sclerosis
Autosomal dominant hyperinsulinism due to SUR1 deficiency
Autosomal recessive hyperinsulinism due to SUR1 deficiency
Congenital analbuminemia
Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency
MODY syndrome
Permanent neonatal diabetes mellitus
Spinocerebellar ataxia type 14
Transient neonatal diabetes mellitus
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
13 OMIM references -
No MeSH references
No signs/symptoms info available.