ODCs

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1 OMIM reference -
1 associated gene
5 signs/symptoms

PROTEIN INTERACTIONS: 1

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

Transient bullous dermolysis of the newborn

Nodulosis-arthropathy-osteolysis syndrome

COL7A1	(UniProt - OMIM)		MMP14	(UniProt - OMIM)
			MMP2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	COL7A1	(0.52)	MMP2

Citations in the biomedical literature:

Transient bullous dermolysis of the newborn		Nodulosis-arthropathy-osteolysis syndrome
	Synonym(s): - DEB, bullous dermolysis of the newborn - DEB-BDN		Synonym(s): - Multicentric osteolysis - nodulosis - arthropathy - NAO syndrome

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: C536979		External references: 2 OMIM references - No MeSH references

Transient bullous dermolysis of the newborn
	Very frequent - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment Frequent - Irregular / patchy skin hypopigmentation - Nails anomalies - Oral mucosa disease / cheilitis - Thin skin
Nodulosis-arthropathy-osteolysis syndrome
(no data available)