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Posterior polar cataract
7 OMIM references -
5 associated genes
123 connected diseases
No signs/symptoms info
Disease Type of connection
Zonular cataract
Nuclear cataract
Coppock-like cataract
Familial isolated dilated cardiomyopathy
Total congenital cataract
Pulverulent cataract
Alpha-crystallinopathy
Cataract-glaucoma
Familial ocular anterior segment mesenchymal dysgenesis
Fatal infantile hypertonic myofibrillar myopathy
Cataract-microcornea syndrome
Cataract with Y-shaped suture opacities
Cerulean cataract
Translocation renal cell carcinoma
Distal hereditary motor neuropathy type 2
Giant cell glioblastoma
Gliosarcoma
Juvenile myelomonocytic leukemia
B-cell chronic lymphocytic leukemia
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
Young adult-onset Parkinsonism
Familial pancreatic carcinoma
Heritable pulmonary arterial hypertension
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Parkinsonian-pyramidal syndrome
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Autosomal dominant Charcot-Marie-Tooth disease type 2L
Hereditary central diabetes insipidus
Idiopathic pulmonary arterial hypertension
Pulmonary venoocclusive disease
Autosomal agammaglobulinemia
Coralliform cataract
Microcephaly-capillary malformation syndrome
SHORT syndrome
LEOPARD syndrome
Metachondromatosis
Noonan syndrome
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Familial gastric cancer
Gastric linitis plastica
Adrenocortical carcinoma
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Craniometaphyseal dysplasia
Essential thrombocythemia
Hypoplastic left heart syndrome
Li-Fraumeni syndrome
Oculodentodigital dysplasia
Papilloma of choroid plexus
Precursor B-cell acute lymphoblastic leukemia
Syndactyly type 3
Mantle cell lymphoma
Multiple myeloma
Muscular dystrophy, Selcen type
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
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 dominant macrothrombocytopenia
Autosomal recessive distal renal tubular acidosis with deafness
Autosomal recessive limb girdle muscular dystrophy type 2A
Autosomal recessive nonsyndromic intellectual deficit
Congenital analbuminemia
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome
Early infantile epileptic encephalopathy
Familial hypocalciuric hypercalcemia type 3
Fetal and neonatal alloimmune thrombocytopenia
Follicular lymphoma
Generalized juvenile polyposis / juvenile polyposis coli
Glanzmann thrombasthenia
Hereditary hemorrhagic telangiectasia
Huntington disease
Inflammatory myofibroblastic tumor
Intravascular large B-cell lymphoma
Juvenile Huntington disease
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
Berardinelli-Seip congenital lipodystrophy
Diffuse cutaneous systemic sclerosis
Limited cutaneous systemic sclerosis
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
Capillary malformation - arteriovenous malformation
Parkes Weber syndrome
Spinocerebellar ataxia type 14
Acrodysostosis
Acrodysostosis with multiple hormone resistance
Carney complex
Familial atrial myxoma
Hereditary sensory and autonomic neuropathy type 5
MODY syndrome
Permanent neonatal diabetes mellitus
Primary pigmented nodular adrenocortical disease
Spinocerebellar ataxia type 26
Synonym(s):
- Posterior subcapsular 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.