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Pulverulent cataract
7 OMIM references -
7 associated genes
169 connected diseases
No signs/symptoms info
Disease Type of connection
Cataract-microcornea syndrome
Nuclear cataract
Coppock-like cataract
Zonular cataract
Cerulean cataract
Posterior polar cataract
Cataract with Y-shaped suture opacities
Young adult-onset Parkinsonism
Amyotrophic lateral sclerosis
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Total congenital cataract
Familial isolated dilated cardiomyopathy
Multiple endocrine neoplasia type 1
Craniometaphyseal dysplasia
Hypoplastic left heart syndrome
Oculodentodigital dysplasia
Syndactyly type 3
Berardinelli-Seip congenital lipodystrophy
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Cystic fibrosis
Epidermolysis bullosa simplex with pyloric atresia
MODY syndrome
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Zollinger-Ellison syndrome
Fatal infantile hypertonic myofibrillar myopathy
Autosomal recessive childhood-onset cortical cataract
Distal hereditary motor neuropathy type 7
Perry syndrome
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
46,XX ovotesticular disorder of sex development
46,XX testicular disorder of sex development
Campomelic dysplasia
Cowden syndrome
Epidermolysis bullosa simplex due to plakophilin deficiency
Proteus syndrome
Acute basophilic leukemia
Autosomal recessive limb-girdle muscular dystrophy type 2Q
Epidermolysis bullosa simplex with muscular dystrophy
Epidermolysis bullosa simplex, Ogna type
Idiopathic pulmonary fibrosis
Keratosis palmoplantaris striata
Lethal acantholytic epidermolysis bullosa
Precursor T-cell acute lymphoblastic leukemia
Skin fragility-woolly hair-palmoplantar keratoderma syndrome
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Distal hereditary motor neuropathy type 2
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Autoimmune lymphoproliferative syndrome with recurrent infections
Autosomal dominant Charcot-Marie-Tooth disease type 2E
Charcot-Marie-Tooth disease type 1F
Severe early-onset axonal neuropathy due to NEFL deficiency
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
Dentatorubral pallidoluysian atrophy
Familial amyloid polyneuropathy
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
Monomelic amyotrophy
Transthyretin-related familial amyloid cardiomyopathy
46,XY complete gonadal dysgenesis
46,XY partial gonadal dysgenesis
Adult-onset autosomal dominant leukodystrophy
Anaplastic ependymoma
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Autosomal recessive spastic paraplegia type 20
Behçet disease
Blau syndrome
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
Extraskeletal Ewing sarcoma
Familial partial lipodystrophy due to AKT2 mutations
Hypohidrotic ectodermal dysplasia with immunodeficiency
Hypoinsulinemic hypoglycemia and body hemihypertrophy
Incontinentia pigmenti
Intermediate nemaline myopathy
Multicentric carpo-tarsal osteolysis with or without nephropathy
Severe congenital nemaline myopathy
Typical nemaline myopathy
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Congenital bilateral absence of vas deferens
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Male infertility with normal virilization due to meiosis defect
Lethal encephalopathy due to mitochondrial and peroxisomal fission defect
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Adult-onset distal myopathy due to VCP mutation
Alexander disease type I
Alexander disease type II
Amish nemaline myopathy
Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
Behavioral variant of frontotemporal dementia
Combined immunodeficiency due to STK4 deficiency
Congenital glaucoma
Coralliform cataract
Dedifferentiated liposarcoma
Distal myopathy with posterior leg and anterior hand involvement
Familial congenital mirror movements
Fibronectin glomerulopathy
Giant cell glioblastoma
Glycogen storage disease due to liver phosphorylase kinase deficiency
Hepatoerythropoietic porphyria
Hereditary breast and ovarian cancer syndrome
Hyperinsulinism due to HNF1A deficiency
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Inherited acute myeloid leukemia
Juvenile glaucoma
Juvenile myelomonocytic leukemia
Keratoderma hereditarium mutilans with ichthyosis
Melanoma of soft part
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Microphthalmia - cataract
Muscle filaminopathy
Muscular dystrophy, Selcen type
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Osteogenesis imperfecta type 3
Perlman syndrome
Pontocerebellar hypoplasia type 1
Porphyria cutanea tarda
Progressive non-fluent aphasia
Progressive symmetric erythrokeratodermia
Pseudohypoaldosteronism type 2E
Richieri Costa-Pereira syndrome
Semantic dementia
Spastic paraplegia - Paget disease of bone
Treacher-Collins syndrome
Well-differentiated liposarcoma
Wolf-Hirschhorn syndrome
X-linked epilepsy - learning disabilities - behavior disorders
Aneurysm - osteoarthritis syndrome
Familial thoracic aortic aneurysm and aortic dissection
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
Spinocerebellar ataxia type 12
17p13.3 microduplication syndrome
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Diffuse cutaneous systemic sclerosis
Distal 17p13.3 microdeletion syndrome
Heritable pulmonary arterial hypertension
Limited cutaneous systemic sclerosis
Miller-Dieker syndrome
Acute promyelocytic leukemia
Autosomal dominant hyperinsulinism due to SUR1 deficiency
Autosomal recessive hyperinsulinism due to SUR1 deficiency
Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency
Generalized junctional epidermolysis bullosa, non-Herlitz type
Junctional epidermolysis bullosa - pyloric atresia
Localized junctional epidermolysis bullosa, non-Herlitz type
Parkinsonian-pyramidal syndrome
Permanent neonatal diabetes mellitus
Spinocerebellar ataxia type 14
Transient neonatal diabetes mellitus
Isolated focal cortical dysplasia type IIb
Tuberous sclerosis
- Dusty 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:
7 OMIM references -
No MeSH references

No signs/symptoms info available.