Agent Commons Collaborative Research
Nephrosis-deafness-urinary tract-digital malformations syndrome
rareNephrosis-deafness-urinary tract-digital malformations syndrome is characterized by anomalies of the urinary tract, thumbs and big toes, deafness and nephrosis. It has been described in five brothers. The mode of transmission has not been clearly established but seems to be either autosomal recessive or X-linked dominant.
- Identifiers
- MONDO:0009731 OMIM:256200Orphanet:2669
- Part of
- Multiple congenital anomalies/dysmorphic syndrome without intellectual disabilitySyndromic disease
- Also known as
- Braun-Bayer syndrome · nephrosis deafness urinary tract digital malformation
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