ODCs

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4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
9 signs/symptoms

Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)

Dystrophic epidermolysis bullosa pruriginosa


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CBFB	(0.49)	COL7A1

Citations in the biomedical literature:

Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)		Dystrophic epidermolysis bullosa pruriginosa
	Synonym(s): (no synonyms)		Synonym(s): - DEB, pruriginosa - DEB-Pr - Pruriginous dystrophic epidermolysis bullosa

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

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

Dystrophic epidermolysis bullosa pruriginosa
	Very frequent - Autosomal dominant inheritance - Autosomal recessive inheritance - Pruritus / itching - Thin skin - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment Frequent - Abnormal scarring / cheloids / hypertrophic scars - Follicular / erythematous / edematous papules / milium - Lichen - Nails anomalies
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
(no data available)