Cytoscape Web
Click node...


13 OMIM references -
10 associated genes
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
1 associated gene
18 signs/symptoms
Nuclear cataract
Nance-Horan syndrome

CRYAA NHS
CRYBB1
CRYBB2
CRYBB3
CRYGD
FYCO1
GJA3
MIP
NHS
WFS1


COMMON
GENES
NHS



Citations in the biomedical literature:


Nuclear cataract
CRYAA CRYBB1 CRYBB2 CRYBB3 CRYGD FYCO1
GJA3 MIP NHS WFS1
Nance-Horan syndrome



Nuclear cataract
Nance-Horan syndrome

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare odontologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
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
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: x-linked dominant

External references:
13 OMIM references -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C538336

Nance-Horan syndrome

Very frequent
- Anomalies of teeth and dentition
- Cataract / lens opacification
- High nasal bridge
- Long face
- Long / large / bulbous nose
- Microcornea
- Nystagmus
- Prognathism / prognathia
- Visual loss / blindness / amblyopia

Frequent
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Metacarpal anomalies / Archibald's sign
- Prominent / bat ears
- Strabismus / squint
- Supernumerary teeth / polyodontia

Occasional
- Anophthalmos / anophthalmia / microphthalmos / microphthalmia
- Glaucoma
- Psychic / behavioural troubles
- Retinal detachment


Nuclear cataract

(no data available)