Dentistry · Dentistry / Pediatric dentistry
Amelogenesis imperfecta with nephrocalcinosis syndrome
also: Enamel-renal syndrome
Amelogenesis imperfecta with nephrocalcinosis.
- Specialty
- Dentistry
- Subspecialty
- Dentistry / Pediatric dentistry
- Sex & age distribution
- Male: affected; Female: affected; Children: yes
- Gene(s) involved
- FAM20A
- Alternative names & eponyms
- Enamel-renal syndrome
Etiology & mechanism
FAM20A mutation.
Gene(s) involved (1)
Symptoms & signs (3)
In plain terms, someone with Amelogenesis imperfecta with nephrocalcinosis syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
Drag nodes, scroll to zoom, click a node to open that syndrome.
Shares symptoms with
1 shared
Autoimmune polyglandular syndrome type 1
enamel hypoplasia
1 shared
Bartter syndrome
nephrocalcinosis
1 shared
Michelis–Castrillo syndrome
nephrocalcinosis
1 shared
Oculodentodigital dysplasia syndrome
enamel hypoplasia
1 shared
Robinow syndrome
gingival hyperplasia
1 shared
Tricho-dento-osseous syndrome
enamel hypoplasia
Shares genes with
None.
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