MYH9 disorder with Döhle-like inclusions, nephritis, deafness and cataracts.
- Specialty
- Nephrology
- Subspecialty
- Nephrology / Hereditary kidney disease
- Sex & age distribution
- Male: affected; Female: affected; Children: yes
- Gene(s) involved
- MYH9
- Alternative names & eponyms
- MYH9-related disease
Etiology & mechanism
MYH9 variants.
Gene(s) involved (1)
Symptoms & signs (5)
In plain terms, someone with Fechtner 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.
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Shares symptoms with
2 shared
Sebastian syndrome
leukocyte inclusions, macrothrombocytopenia
1 shared
Chanarin–Dorfman syndrome
cataracts
1 shared
Congenital rubella syndrome
deafness
1 shared
DRESS syndrome
nephritis
1 shared
Epstein syndrome
macrothrombocytopenia
1 shared
GATA2 deficiency syndrome
deafness
1 shared
Gray platelet syndrome
macrothrombocytopenia
1 shared
Henoch–Schönlein purpura syndrome
nephritis
1 shared
Johanson–Blizzard syndrome
deafness
1 shared
Kallmann syndrome with neurological involvement
deafness
Shares genes with
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