Cytoscape Web
Click node...

Peters anomaly
1 OMIM reference -
6 associated genes
143 connected diseases
12 signs/symptoms
Disease Type of connection
Axenfeld anomaly
Axenfeld-Rieger syndrome
Rieger anomaly
Familial thoracic aortic aneurysm and aortic dissection
Familial atrial fibrillation
Ring dermoid of cornea
Aniridia - cerebellar ataxia - intellectual deficit
Autosomal dominant keratitis
Congenital glaucoma
Foveal hypoplasia - presenile cataract
Isolated aniridia
Isolated optic nerve hypoplasia
Juvenile glaucoma
Morning glory syndrome
WAGR syndrome
Isolated anophthalmia - microphthalmia
Precursor B-cell acute lymphoblastic leukemia
Colobomatous microphthalmia
Septo-optic dysplasia
Waardenburg syndrome type 2
Loeys-Dietz syndrome type 1
Anophthalmia / microphthalmia - esophageal atresia
Coffin-Siris syndrome
Familial rhabdoid tumor
Familial cerebral saccular aneurysm
Aneurysm - osteoarthritis syndrome
Familial pancreatic carcinoma
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Clear cell renal carcinoma
MITF-related melanoma and renal cell carcinoma predisposition syndrome
Ocular albinism with congenital sensorineural deafness
Papillary renal cell carcinoma
Tietz syndrome
Spinocerebellar ataxia type 17
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Partial androgen insensitivity syndrome
Follicular lymphoma
Intravascular large B-cell lymphoma
Primary mediastinal large B-cell lymphoma
Autosomal dominant nonsyndromic intellectual deficit
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Hereditary nonpolyposis colon cancer
Marfan syndrome type 2
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Microphthalmia - cataract
Miller-Dieker syndrome
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Chronic myelomonocytic leukemia
Congenital mesoblastic nephroma
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
2q37 microdeletion syndrome
Alobar holoprosencephaly
Camurati-Engelmann disease
Chronic intestinal pseudoobstruction
Congenital hereditary facial paralysis with variable hearing loss
Congenital short bowel syndrome
Congenital stromal corneal dystrophy
Congenital valvular dysplasia
Cystic fibrosis
Ehlers-Danlos syndrome with periventricular heterotopia
Familial retinoblastoma
Frontometaphyseal dysplasia
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Monosomy 13q14
Osteodysplasty, Melnick-Needles type
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Periventricular nodular heterotopia
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Terminal osseous dysplasia - pigmentary defects
Unilateral retinoblastoma
5q14.3 microdeletion syndrome
Aicardi-Goutières syndrome
Athabaskan brainstem dysgenesis syndrome
Bosley-Salih-Alorainy syndrome
Cornelia de Lange syndrome
Dyschromatosis symmetrica hereditaria
Familial infantile bilateral striatal necrosis
Idiopathic hypereosinophilic syndrome
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
Papillary or follicular thyroid carcinoma
X-linked dystonia-parkinsonism
Immunodeficiency by defective expression of HLA class 2
Lennox-Gastaut syndrome
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Adrenocortical carcinoma
Autosomal recessive axonal neuropathy with neuromyotonia
B-cell chronic lymphocytic leukemia
Burkitt lymphoma
Essential thrombocythemia
Familial isolated dilated cardiomyopathy
Giant cell glioblastoma
Inherited acute myeloid leukemia
Kallmann syndrome
Li-Fraumeni syndrome
Myhre syndrome
Neurologic Waardenburg-Shah syndrome
Papilloma of choroid plexus
Precursor T-cell acute lymphoblastic leukemia
Waardenburg-Shah syndrome
Multiple keratoacanthoma, Ferguson-Smith type
Estrogen resistance syndrome
20p12.3 microdeletion syndrome
46,XX testicular disorder of sex development
Acute promyelocytic leukemia
Brachydactyly type A2
Combined pituitary hormone deficiencies, genetic forms
Diffuse cutaneous systemic sclerosis
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
Limited cutaneous systemic sclerosis
Monosomy 22q13
X-linked congenital generalized hypertrichosis
X-linked intellectual deficit with isolated growth hormone deficiency
Hereditary sensory and autonomic neuropathy type 2
Pseudohypoaldosteronism type 2C
Williams syndrome
- Peters congenital glaucoma

Classification (Orphanet):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C537884

Very frequent
- Anomalies of eyes and vision
- Autosomal recessive inheritance
- Microcornea

- Corneal dystrophy

- Anomalies of teeth and dentition
- Anophthalmos / anophthalmia / microphthalmos / microphthalmia
- Aphakia / microphakia / spherophakia / biphakia / absence of lens / lenticone / lentiglobus
- Cataract / lens opacification
- Corneal clouding / opacity / vascularisation
- Dental malocclusion
- Hypoplastic mandibula / partial absence of the mandibula
- Nystagmus