MSeqDR Mitochondrial Disease Portal


 
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Parent Node:
expandimmune system disease (MONDO:0005046)
Parent Node:
expandskin disease (MONDO:0005093)
..Starting node
..expandimmune deficiency with skin involvement ()

       Child Nodes:
........expandagammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome ()
........expandChediak-Higashi syndrome ()
........expandchronic granulomatous disease ()
........expandchronic mucocutaneous candidiasis (disease) ()
........expandcombined immunodeficiency with skin granulomas ()
........expandepidermodysplasia verruciformis ()
........expanderythroderma desquamativum ()
........expandGriscelli syndrome type 2 ()
........expandhereditary mucoepithelial dysplasia ()
........expandHyper-IgE recurrent infection syndrome 1 ()
........expandWiskott-Aldrich syndrome ()



 Sister Nodes: 
..expandAchenbach syndrome ()
..expandaquagenic pruritus ()
..expandautoimmune disease with skin involvement ()
..expandBorrone di Rocco Crovato syndrome ()
..expandchronic ulcer of skin ()
..expandcutaneous mucinosis ()
..expandcutaneous sclerosis ()
..expanddermatitis ()
..expandepidermal appendage anomaly ()
..expanderythema multiforme ()
..expanderythematosquamous dermatosis ()
..expandexanthem (disease) ()
..expandfacial dermatosis ()
..expandgenetic photodermatosis ()
..expandgenetic skin disease ()
..expandhand dermatosis ()
..expandhematohidrosis ()
..expandhordeolum ()
..expandhyperglobulinemic purpura ()
..expandimmune deficiency with skin involvement ()
..expandinflammatory skin disease ()
..expandkeratosis ()
..expandkeratosis pilaris ()
..expandKimura disease ()
..expandleg dermatosis ()
..expandlichen disease ()
..expandlipodystrophy (disease) ()
..expandlivedoid vasculopathy ()
..expandmetabolic disease with skin involvement ()
..expandmongolian spot ()
..expandnecrobiosis lipoidica ()
..expandnon-neoplastic nevus ()
..expandother acquired skin disease ()
..expandother genetic dermis disorder ()
..expandother genetic epidermal disease ()
..expandparonychia (disease) ()
..expandpityriasis rotunda ()
..expandpremature aging ()
..expandprurigo nodularis ()
..expandpyoderma ()
..expandrare epidermal disease ()
..expandrare photodermatosis ()
..expandreactive cutaneous fibrous lesion ()
..expandrosacea ()
..expandscalp dermatosis ()
..expandsclerema neonatorum ()
..expandsebaceous gland disease ()
..expandsevere cutaneous adverse reaction ()
..expandskin atrophy ()
..expandskin disease caused by infection ()
..expandskin neoplasm ()
..expandskin pigmentation disease ()
..expandskin sarcoidosis ()
..expandskin vascular disease ()
..expandsunburn ()
..expandsweat gland disease ()
..expandtoxic dermatosis ()
..expandunclassified genetic skin disorder ()
..expandvesiculobullous skin disease ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:19305
Name:immune deficiency with skin involvement
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal