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X-linked Opitz G/BBB syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Acute myeloblastic leukemia with maturation
3 associated genes
No signs/symptoms info
X-linked Opitz G/BBB syndrome
Acute myeloblastic leukemia with maturation

MID1
(UniProt - OMIM)
 FLT3
(UniProt - OMIM)
KIT
(UniProt - OMIM)
NPM1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MID1
(0.63)
NPM1


Citations in the biomedical literature:


X-linked Opitz G/BBB syndrome
MID1
Acute myeloblastic leukemia with maturation
FLT3 KIT NPM1



X-linked Opitz G/BBB syndrome
Acute myeloblastic leukemia with maturation

Synonym(s):
- X-linked Opitz BBB/G syndrome
- X-linked Opitz syndrome
- XLOS
Synonym(s):
- Acute myeloblastic leukemia type 2
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
- Rare urogenital disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.