Cytoscape Web
Click node...

Zonular cataract
9 OMIM references -
9 associated genes
91 connected diseases
No signs/symptoms info
Disease Type of connection
Cataract-microcornea syndrome
Nuclear cataract
Coppock-like cataract
Cerulean cataract
Cataract with Y-shaped suture opacities
Total congenital cataract
Familial isolated dilated cardiomyopathy
Pulverulent cataract
Posterior polar cataract
Alpha-crystallinopathy
Fatal infantile hypertonic myofibrillar myopathy
Coralliform cataract
Anterior polar cataract
Microphthalmia - cataract
Distal hereditary motor neuropathy type 2
Autosomal dominant Charcot-Marie-Tooth disease type 2F
B-cell chronic lymphocytic leukemia
Familial pancreatic carcinoma
Follicular lymphoma
Intravascular large B-cell lymphoma
Congenital analbuminemia
Parkinsonian-pyramidal syndrome
Young adult-onset Parkinsonism
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
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
Autosomal dominant Charcot-Marie-Tooth disease type 2L
Hereditary central diabetes insipidus
Heritable pulmonary arterial hypertension
Idiopathic pulmonary arterial hypertension
Pulmonary venoocclusive disease
Familial gastric cancer
Gastric linitis plastica
Adrenocortical carcinoma
Essential thrombocythemia
Giant cell glioblastoma
Gliosarcoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Precursor B-cell acute lymphoblastic leukemia
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Primary mediastinal large B-cell lymphoma
Distal 22q11.2 microdeletion syndrome
Mantle cell lymphoma
Multiple myeloma
Catecholaminergic polymorphic ventricular tachycardia
Coffin-Siris syndrome
Familial rhabdoid tumor
Muscular dystrophy, Selcen type
Autosomal recessive centronuclear myopathy
Autosomal recessive limb-girdle muscular dystrophy type 2J
Early-onset myopathy with fatal cardiomyopathy
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Hereditary proximal myopathy with early respiratory failure
Tibial muscular dystrophy
Autoimmune lymphoproliferative syndrome with recurrent infections
Autosomal recessive limb girdle muscular dystrophy type 2A
Autosomal recessive nonsyndromic intellectual deficit
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Myhre syndrome
Papillary or follicular thyroid carcinoma
X-linked hyper-IgM syndrome
X-linked lymphoproliferative disease
Alexander disease type I
Alexander disease type II
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16
Amyotrophic lateral sclerosis
Autosomal dominant beta2-microglobulinic amyloidosis
Autosomal dominant limb-girdle muscular dystrophy type 1E
Autosomal dominant methemoglobinemia
Autosomal recessive limb-girdle muscular dystrophy due to desmin deficiency
Desminopathy
Familial apolipoprotein C-II deficiency
Hb Bart's hydrops fetalis
Hemoglobin H disease
Scapuloperoneal amyotrophy
Hereditary sensory and autonomic neuropathy type 5
MODY syndrome
Permanent neonatal diabetes mellitus
Synonym(s):
- Lamellar cataract
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
9 OMIM references -
1 MeSH reference: C535342
No signs/symptoms info available.