ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
35 signs/symptoms

Hypohidrotic ectodermal dysplasia with immunodeficiency

Nakajo-Nishimura syndrome

IKBKG	(UniProt - OMIM)		PSMB8	(UniProt - OMIM)
NFKBIA	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	IKBKG	(0.63)	PSMB8

Citations in the biomedical literature:

Hypohidrotic ectodermal dysplasia with immunodeficiency		Nakajo-Nishimura syndrome
	Synonym(s): - Anhidrotic ectodermal dysplasia with immunodeficiency - EDA-ID - HED-ID		Synonym(s): - Amyotrophy - fat tissue anomaly - NNS - Secondary hypertrophic osteoperiostosis with pernio

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare immune disease - Rare skin disease		Classification (Orphanet): - Rare genetic disease - Rare skin disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Diseases of the skin and subcutaneous tissue -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: child / adolescent Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: childhood Average age of death: young adult Type of inheritance: autosomal recessive

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

Nakajo-Nishimura syndrome
	Very frequent - Abnormal fat distribution / lipodystrophy - Arthrogryposis - Articular / joint pain / arthralgia - Autosomal recessive inheritance - Biological inflammatory syndrome / increased erythrocyte sedimentation rate / CRP - Cutaneous rash - Erythema / erythematous lesions / erythroderma / polymorphous erythema - Face / facial anomalies - Fever / chilling - Hepatomegaly / liver enlargement (excluding storage disease) - Hyperostosis - Lipoatrophy - Restricted joint mobility / joint stiffness / ankylosis - Splenomegaly - Subcutaneous nodules / lipomas / tumefaction / swelling Frequent - Hypergammaglobulinemia - Hyperhidrosis / increased sweating - Lymphadenopathy / polyadenopathies - Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy - Muscle weakness / flaccidity - Terminal broadening / clubbing of toes - Thick / dowel fingers Occasional - Cardiac conduction defect / sinoauricular / heart / auriculoventricular / branch block - Cardiac rhythm disorder / arrhythmia - Cardiomegaly - Heart / cardiac failure - Intellectual deficit / mental / psychomotor retardation / learning disability - Long hand / arachnodactyly - Long / large ear - Long / large / bulbous nose - Macroglossia / tongue protrusion / proeminent / hypertrophic - Microcytic anemia - Pyramidal syndrome - Respiratory distress / dyspnea / respiratory failure / lung volume reduction - Thick lips
Hypohidrotic ectodermal dysplasia with immunodeficiency
(no data available)