Cytoscape Web
Click node...


7 OMIM references -
8 associated genes
5 signs/symptoms
PROTEIN INTERACTIONS: 2
1 OMIM reference -
7 associated genes
No signs/symptoms info
46,XY complete gonadal dysgenesis
Acute promyelocytic leukemia

CBX2 NABP1
DHH NPM1
DMRT1 NUMA1
DMRT2 PML
MAP3K1 RARA
NR0B1 STAT5B
NR5A1 ZBTB16
SRY


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CBX2
MAP3K1
(0.72)
(0.56)
NPM1
RARA



Citations in the biomedical literature:


46,XY complete gonadal dysgenesis
CBX2 DHH DMRT1 DMRT2 MAP3K1 NR0B1
NR5A1 SRY
Acute promyelocytic leukemia
NABP1 NPM1 NUMA1 PML RARA STAT5B
ZBTB16



46,XY complete gonadal dysgenesis
Acute promyelocytic leukemia

Synonym(s):
- 46,XY CGD
- 46,XY pure gonadal dysgenesis
- Swyer syndrome

Synonym(s):
- Acute myeloblastic leukemia type 3
- Acute myeloid leukemia with t(15;17)(q22;q12);(PML/RARalpha) and variants

Classification (Orphanet):
- Rare cardiac disease
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare skin 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:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
7 OMIM references -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D015473

46,XY complete gonadal dysgenesis

Very frequent
- Abnormal / polycystic ovaries
- Late puberty / hypogonadism / hypogenitalism
- Male pseudohermaphrodism / lack of virilisation
- Small / atrophic / hypoplastic testes / monorchism / microorchidism / anorchia
- X-linked recessive inheritance



Acute promyelocytic leukemia

(no data available)