Endocrinology · Endocrinology / Pediatric endocrinology
Kagami–Ogata syndrome
also: Paternal UPD14 syndrome
Imprinting disorder with bell-shaped thorax and polyhydramnios.
- Specialty
- Endocrinology
- Subspecialty
- Endocrinology / Pediatric endocrinology
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes, perinatal
- Gene(s) involved
- DLK1, MEG3, RTL1
- Alternative names & eponyms
- Paternal UPD14 syndrome
Etiology & mechanism
Paternal UPD14.
Gene(s) involved (3)
Symptoms & signs (6)
In plain terms, someone with Kagami–Ogata 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
Acute respiratory distress syndrome
respiratory failure
1 shared
Aicardi syndrome
developmental delay
1 shared
Bannayan–Riley–Ruvalcaba syndrome
developmental delay
1 shared
Bartter syndrome
polyhydramnios
1 shared
Brain–lung–thyroid syndrome
developmental delay
1 shared
Cardio-facio-cutaneous syndrome
developmental delay
1 shared
Chanarin–Dorfman syndrome
developmental delay
1 shared
Cobalamin C syndrome
developmental delay
1 shared
Cockayne syndrome
developmental delay
1 shared
Congenital chloride diarrhea syndrome
polyhydramnios
Shares genes with
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