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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
leukocyte disease +     
skin disease +     
Abnormal Neutrophil Chemotactic Response 
Achenbach syndrome 
acidophil adenoma 
Acneiform Eruptions +   
adiaspiromycosis 
aggressive NK-cell leukemia 
allergic cutaneous vasculitis +   
ancylostomiasis +  
autoimmune disease of skin and connective tissue +   
B-cell lymphoma +   
basophil adenoma 
basophilic adenocarcinoma 
Birt-Hogg-Dube syndrome  
BOCKENHEIMER SYNDROME  
Bone Tissue Neoplasms +   
Boudhina Yedes Khiari syndrome 
breast disease +   
C syndrome  
Cd4+ Lymphocyte Deficiency  
cercarial dermatitis 
chancroid +  
chondroma +   
chronic ulcer of skin +   
clear cell sarcoma +   
coenurosis 
connective tissue benign neoplasm +   
connective tissue cancer +   
contagious pustular dermatitis 
Cutaneous Fistula 
cutaneous lupus erythematosus +   
cutis laxa +   
dendritic cell sarcoma +   
Dermal Fibrosis  
dermatitis +   
Dermatoleukodystrophy 
dermatomyositis +   
dipetalonemiasis 
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
Ectodermal Dysplasia-Skin Fragility Syndrome  
Eczematous Skin Diseases +   
Elastosis Perforans Serpiginosa 
Elliott Ludman Teebi Syndrome 
endometrial stromal tumor +   
endometriosis in scar of skin 
Eosinophilia +   
epidermal nevus +   
Erythema +   
erythematosquamous dermatosis 
exanthem +   
eyelid disease +   
FACES Syndrome 
facial dermatosis +   
Fibrous Tissue Neoplasms +   
filariasis +   
Flynn Aird Syndrome 
Foot Diseases +   
Frank-Ter Haar syndrome  
gastrointestinal stromal tumor +   
Genetic Skin Diseases +   
Giant Cell Tumors +   
granulomatosis with polyangiitis +   
hair disease +   
hand dermatosis +  
hemorrhoid +   
hereditary neutrophilia  
Hernandez Fragoso Syndrome 
ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis  
IMMUNODEFICIENCY 108 WITH AUTOINFLAMMATION  
immunodeficiency 32B  
immunodeficiency 7  
infectious mononucleosis  
Infectious Skin Diseases +   
juvenile xanthogranuloma 
keratosis +   
Kimura disease 
Lazy Leukocyte Syndrome  
leg dermatosis 
leukocyte adhesion deficiency +   
Leukocyte Nuclear Appendages, Hereditary Prevalence of 
Leukocytosis +   
leukopenia +   
leukostasis  
lipomatosis +   
localized scleroderma +   
loiasis 
Macroepiphyseal Dysplasia, McAlister Coe Type 
MASS Syndrome  
mastocytosis +   
A heterogenous group of disorders characterized by the abnormal increase of MAST CELLS in only the skin (MASTOCYTOSIS, CUTANEOUS), in extracutaneous tissues involving multiple organs (MASTOCYTOSIS, SYSTEMIC), or in solid tumors (MASTOCYTOMA).
Median Cleft Lip, Corpus Callosum, Lipoma, and Skin Polyps 
Mental Retardation, Joint Hypermobility, and Skin Laxity, with or without Metabolic Abnormalities 
Metabolic Skin Diseases +   
mongolian spot 
Monocyte Esterase Deficiency  
Morgellons Disease 
multicentric reticulohistiocytosis 
multiple cutaneous and mucosal venous malformations  
Myxoma +   
nail disease +   
necrobiosis lipoidica 
Necrobiotic Disorders +  
Necrolytic Migratory Erythema 
Nephrogenic Fibrosing Dermopathy  
Neurodevelopmental Disorder with Facial Dysmorphism, Absent Language, and Pseudo-Pelger-Huet Anomaly  
Neutrophil Actin Dysfunction 
noninfectious dermatoses of eyelid +  
Oncogenic Osteomalacia 
Papulosquamous Skin Diseases +   
Pelger-Huet anomaly +   
phaeohyphomycosis +  
phagocyte bactericidal dysfunction +   
Phagocytosis, Plasma-Related Defect in 
Phosphaturic Mesenchymal Tumor 
photosensitivity disease +   
pigmentation disease +   
Presentey Anomaly  
Prurigo  
Pruritus +   
Pseudoatrophoderma Colli 
Pseudopyogenic Granuloma 
reactive cutaneous fibrous lesion +   
rosacea +   
Roy Maroteaux Kremp Syndrome 
scalp dermatosis +   
sebaceous gland disease +   
Skin Abnormalities +   
skin atrophy 
Skin Neoplasms +   
skin sarcoidosis 
Specific Granule Deficiency +   
sweat gland disease +   
synovial sarcoma +   
T-Cell OKT4 Deficiency  
tyrosinemia type II  
Undritz Anomaly 
Upton Young Syndrome 
vascular skin disease +   
verruciform xanthoma of skin 
XEROSIS AND GROWTH FAILURE WITH IMMUNE AND PULMONARY DYSFUNCTION SYNDROME  

Synonyms
Exact Synonyms: Mast Cell Disease ;   Mast-Cell Diseases ;   Mastocytoses ;   mast cell hyperplasia
Narrow Synonyms: MASTOCYTOSIS URTICARIA PIGMENTOSA ;   MASTOCYTOSIS, SPORADIC, CHILDHOOD-ONSET ;   Mastocytosis, Adult Sporadic ;   mastocytosis with associated hematologic disorder
Primary IDs: MESH:D008415
Alternate IDs: MIM:154800
Xrefs: EFO:0009001 ;   GARD:6987 ;   ICD10CM:Q82.2 ;   NCI:C84269
Definition Sources: MESH:D008415

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