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Gyrate atrophy of choroid and retina
1 OMIM reference -
1 associated gene
9 connected diseases
No signs/symptoms info
Disease Type of connection
Burkitt lymphoma
Precursor T-cell acute lymphoblastic leukemia
Autosomal dominant hypohidrotic ectodermal dysplasia
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Craniometaphyseal dysplasia
Hypoplastic left heart syndrome
Oculodentodigital dysplasia
Syndactyly type 3
Galactosialidosis
Synonym(s):
- HOGA
- Hyperornithinemia
- Hyperornithinemia - gyrate atrophy of choroid and retina
- Ornithine aminotransferase deficiency
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
1 MeSH reference: C537132
Gene symbol UniProt reference OMIM reference
OAT P04181613349
No signs/symptoms info available.