ODCs

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4 associated genes
No signs/symptoms info

COMMON GENES: 1

1 associated gene
3 signs/symptoms

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

Pseudoxanthomatous diffuse cutaneous mastocytosis

Citations in the biomedical literature:

Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)		Pseudoxanthomatous diffuse cutaneous mastocytosis
	Synonym(s): (no synonyms)		Synonym(s): - Infiltrative small vesicular DCM - Infiltrative small vesicular diffuse cutaneous mastocytosis - Pseudoxanthomatous DCM

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare allergic disease - Rare hematologic disease - Rare oncologic 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: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: sporadic

	External references: No OMIM references No MeSH references		External references: No OMIM references No MeSH references

Pseudoxanthomatous diffuse cutaneous mastocytosis
	Very frequent - Dermal / subcutaneous infiltration / induration - Mastocytosis - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
(no data available)