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Congenital pulmonary alveolar proteinosis

5 OMIM references -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

Bullous diffuse cutaneous mastocytosis

1 associated gene
7 signs/symptoms

Congenital pulmonary alveolar proteinosis

Bullous diffuse cutaneous mastocytosis

ABCA3	(UniProt - OMIM)		KIT	(UniProt - OMIM)
CSF2RA	(UniProt - OMIM)
CSF2RB	(UniProt - OMIM)
SFTPB	(UniProt - OMIM)
SFTPC	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CSF2RA CSF2RB	(0.52) (0.52)	KIT KIT

Citations in the biomedical literature:

Congenital pulmonary alveolar proteinosis		Bullous diffuse cutaneous mastocytosis
	Synonym(s): - Congenital PAP		Synonym(s): - Bullous DCM

	Classification (Orphanet): - Rare genetic disease - Rare respiratory disease		Classification (Orphanet): - Rare allergic disease - Rare hematologic disease - Rare oncologic disease - Rare skin disease

	Classification (ICD10): - Diseases of the respiratory system -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: sporadic

	External references: 5 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

Bullous diffuse cutaneous mastocytosis
	Very frequent - Abnormal pigmentary skin changes / skin pigmentation anomalies - Erythema / erythematous lesions / erythroderma / polymorphous erythema - Mastocytosis - Pruritus / itching - Urticaria - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment Occasional - Collapse / sudden death / cardiac arrest / cardiorespiratory arrest
Congenital pulmonary alveolar proteinosis
(no data available)