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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Pathologic Processes (D010335)
Parent Node: Skin Diseases, Vesiculobullous (D012872)
..Starting node ..Acantholysis (D000051)
Child Nodes:
........Grover's disease (C537306)
Sister Nodes:
..Acantholysis (D000051) 1
..Amyloidosis, Cutaneous Bullous (C562644)
..Atrichia with Papular Lesions (C565924)
..Blister (D001768) 3
..Dermatitis Herpetiformis (D003874) 1
..Eczema, Dyshidrotic (D011146)
..Eosinophilic pustular folliculitis (C535953)
..Epidermolysis Bullosa (D004820) 29
..Erythema Multiforme (D004892) 1
..Hydroa Vacciniforme (D006837) 1
..Linear IgA Bullous Dermatosis (D062027)
..Papular urticaria (C537169)
..Pemphigoid Gestationis (D006559)
..Pemphigoid, Benign Mucous Membrane (D010390)
..Pemphigoid, Bullous (D010391)
..Pemphigus (D010392) 2
..Pemphigus, Benign Familial (D016506)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	113
Name:	Acantholysis
Definition:	Separation of the prickle cells of the stratum spinosum of the epidermis, resulting in atrophy of the prickle cell layer. It is seen in diseases such as pemphigus vulgaris (see PEMPHIGUS) and DARIER DISEASE.
Alternative IDs:
ParentIDs:	MESH:D010335\|MESH:D012872
TreeNumbers:	C17.800.865.070 \|C23.550.035
Synonyms:	Acantholyses
Slim Mappings:	Pathology (process)\|Skin disease
Reference:	MedGen: D000051 MeSH: D000051 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants