Nephrology · Nephrology / Congenital anomalies of kidney and urinary tract
Fraser syndrome
also: Cryptophthalmos syndrome
Cryptophthalmos, syndactyly and renal agenesis.
- Specialty
- Nephrology
- Subspecialty
- Nephrology / Congenital anomalies of kidney and urinary tract
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes, prenatal
- Gene(s) involved
- FRAS1, FREM2, GRIP1
- Alternative names & eponyms
- Cryptophthalmos syndrome
Etiology & mechanism
Basement membrane adhesion defects.
Gene(s) involved (3)
Symptoms & signs (6)
In plain terms, someone with Fraser 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
Apert syndrome
syndactyly
1 shared
Branchio-oto-renal syndrome
renal agenesis
1 shared
Denys–Drash syndrome
ambiguous genitalia
1 shared
Herlyn–Werner–Wunderlich syndrome
renal agenesis
1 shared
Kallmann syndrome
renal agenesis
1 shared
LEOPARD syndrome
genital anomalies
1 shared
Noonan syndrome with multiple lentigines
genital anomalies
1 shared
Oculodentodigital dysplasia syndrome
syndactyly
1 shared
Orofaciodigital syndrome type 1
syndactyly
1 shared
Potocki–Shaffer syndrome
syndactyly
Shares genes with
None.
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