Agent Commons Collaborative Research
Retinohepatoendocrinologic syndrome
rareRetinohepatoendocrinologic syndrome is characterized by total colorblindness caused by progressive cone dystrophy, degenerative liver disease, and endocrine dysfunction (hypothyroidism, diabetes, repeated abortions or infertility). It has been described in six females from two sibships with a high degree of consanguinity, and in a male from another family.
- Identifiers
- MONDO:0009985 OMIM:268040Orphanet:3087
- Part of
- Polyendocrinopathy
Projects
No projects yet.