| 疾病名称 |
别名 |
|
| Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, And Acne |
|
Papa Syndrome
|
Fra
|
|
Familial Recurrent Arthritis
|
Pyogenic Arthritis, Pyoderma Gangrenosum And Acne
|
|
PAPAS
|
Pyogenic Arthritis-Pyoderma Gangrenosum-Acne Syndrome
|
|
Pyogenic Arthritis, Pyoderma Gangrenosum, And Severe Cystic Acne
|
Pyogenic Sterile Arthritis, Pyoderma Gangrenosum And Acne
|
|
|
| Zinc, Elevated Plasma |
|
Albumin Binding Of Zinc, Elevated
|
Hyperzincemia, Familial Dysalbuminemic
|
|
Hyperzincemia And Hypercalprotectinemia
|
Hz/Hc
|
|
Pami Syndrome
|
Pstpip1-Associated Myeloid-Related Proteinemia Inflammatory Syndrome
|
|
|
| Behcet Syndrome |
|
Behcet Disease
|
Behcet'S Syndrome
|
|
Behcet'S Disease
|
Behçet Disease
|
|
Bd
|
Adamantiades-Behcet Disease
|
|
Triple Symptom Complex
|
Behçet'S Disease
|
|
Behet'S Syndrome
|
Bd Syndrome
|
|
Behçet Syndrome
|
Behçet'S Syndrome
|
|
Behcet Triple Symptom Complex
|
Malignant Aphthosis
|
|
Old Silk Route Disease
|
Adamantiades-Behçet Disease
|
|
|
| Pyoderma Gangrenosum |
|
Phagedenic Pyoderma
|
Phagedena Geometric
|
|
|
| Pyoderma |
|
|
| Acne |
|
Acne Vulgaris
|
Acne Varioliformis
|
|
Frontalis Acne
|
|
|
| Familial Mediterranean Fever |
|
Periodic Fever Syndrome
|
FMF
|
|
Benign Paroxysmal Peritonitis
|
Periodic Disease
|
|
Recurrent Polyserositis
|
Familial Paroxysmal Polyserositis
|
|
Periodic Fever
|
Familial Mediterranean Fever, Autosomal Recessive
|
|
Familial Mediterranean Fever, Ar
|
Polyserositis, Recurrent
|
|
Polyserositis, Familial Paroxysmal
|
Periodic Peritonitis
|
|
Mef
|
Reimann Periodic Disease
|
|
Siegal-Cattan-Mamou Disease
|
Wolff Periodic Disease
|
|
Benign Recurrent Polyserositis
|
Mediterranean Fever, Familial
|
|
ARFMF
|
Autosomal Recessive Familial Mediterranean Fever
|
|
Fever, Mediterranean, Familial, Autosomal Recessive
|
Hereditary Autoinflammatory Diseases
|
|
Fmf - [Familial Mediterranean Fever]
|
Periodic Polyserositis
|
|
Periodic Familial Polyserositis
|
Periodic Familial Peritonitis
|
|
Paroxysmal Polyserositis
|
Hereditary Amyloid Nephropathy
|
|
Familial Recurrent Polyserositis
|
Familial Non-Neuropathic Amyloidosis
|
|
Armenian Disease
|
Riemann Periodic Disease
|
|
Siegal Cattan Mamou Disease
|
|
|
| Hidradenitis |
|
|
| Hidradenitis Suppurativa |
|
Acne Inversa
|
Suppurative Hidradenitis
|
|
Acne Inversa, Familial
|
Apocrinitis
|
|
Hidradenitides, Suppurative
|
Hidradenitis, Suppurative
|
|
Suppurative Hidradenitides
|
Inverse Acne
|
|
|
| Sebaceous Gland Disease |
|
Sebaceous Gland Anomaly
|
Sebaceous Gland Diseases
|
|
|
| Wiskott-Aldrich Syndrome |
|
WAS
|
Eczema-Thrombocytopenia-Immunodeficiency Syndrome
|
|
Immunodeficiency 2
|
Aldrich Syndrome
|
|
Imd2
|
Wiskott-Aldrich Syndrome 1
|
|
Was1
|
Wiskott Syndrome
|
|
Wiskott Aldrich Syndrome
|
Eczema Thrombocytopenia Immunodeficiency Syndrome
|
|
Imd 2
|
|
|
| Arthritis |
|
Inflammatory Joint Disease
|
Inflammatory Disorder Of Joint
|
|
|
| Sapho Syndrome |
|
Acquired Hyperostosis Syndrome
|
Synovitis, Acne, Pustulosis Palmaris, Hyperostosis, Osteomyelitis Syndrome
|
|
Synovitis Acne Pustulosis Hyperostosis Osteitis
|
Synovitis, Acne, Pustlosis, Hyperostosis, And Osteomyelitis
|
|
Synovitis-Acne-Pustulosis-Hyperostosis-Osteitis Syndrome
|
Synovitis, Acne, Pustulosis, Hyperostosis, And Osteitis Syndrome
|
|
Pustulo-Psoriatic Hyperostotic Spondylarthritis
|
Sapho - [Synovitis, Acne, Pustulosis, Hyperostosis, Osteitis] Syndrome
|
|
|
| Erysipeloid |
|
Infection Due To Erysipelothrix Rhusiopathiae
|
Erysipelothrix Infection
|
|
|
| Erythema Elevatum Diutinum |
|
|
| Mevalonic Aciduria |
|
Mevalonate Kinase Deficiency
|
Mevalonicaciduria
|
|
Hyperimmunoglobulin D With Periodic Fever
|
MEVA
|
|
Complete Mevalonate Kinase Deficiency
|
Mva
|
|
Hyperimmunoglobulinemia D
|
Hyper Igd Syndrome
|
|
Periodic Fever, Dutch Type
|
Mkd
|
|
Aciduria, Mevalonic
|
Deficiency Of Mevalonate Kinase
|
|
|
| Chronic Recurrent Multifocal Osteomyelitis |
|
Chronic Multifocal Osteomyelitis
|
CRMO
|
|
Cmo
|
Cno/Crmo
|
|
Chronic Nonbacterial Osteomyelitis/Chronic Recurrent Multifocal Osteomyelitis
|
Osteomyelitis, Chronic Multifocal
|
|
Multifocal Osteomyelitis, Chronic
|
Chronic Osteomyelitis
|
|
Chronic Multifocal Osteomyelitis, Unspecified Site
|
Crmo - [Chronic Multifocal Osteomyelitis]
|
|
Chronic Osteomyelitis With Draining Sinus, Unspecified Site
|
Bone Fistula With Chronic Osteomyelitis
|
|
|
| Periodic Fever, Familial, Autosomal Dominant |
|
Familial Hibernian Fever
|
Tumor Necrosis Factor Receptor-Associated Periodic Syndrome
|
|
Traps
|
FPF
|
|
Tnf Receptor-Associated Periodic Fever Syndrome
|
Hibernian Fever, Familial
|
|
Fhf
|
Tnf Receptor-Associated Periodic Syndrome
|
|
Autosomal Dominant Familial Periodic Fever
|
Periodic Fever, Familial
|
|
Tnf Receptor 1-Associated Periodic Syndrome
|
Tumor Necrosis Factor Receptor 1 Associated Periodic Syndrome
|
|
Familial Periodic Fever
|
Traps Syndrome
|
|
Tnf Receptor Associated Periodic Syndrome
|
Caledonian Fever
|
|
Fever, Periodic, Familial
|
Tumor Necrosis Factor Receptor 1-Associated Periodic Syndrome
|
|
|
| Sweat Gland Disease |
|
|
| Familial Cold Autoinflammatory Syndrome |
|
Familial Cold Urticaria
|
Fcas
|
|
Familial Polymorphous Cold Eruption
|
Fcu
|
|
Cold Hypersensitivity
|
|
|
| Miliaria Pustulosa |
|
|
| Ludwig'S Angina |
|
Cellulitis Of Floor Of Mouth
|
Ludwig Angina
|
|
|
| Periostitis |
|
|
| Familial Cold Autoinflammatory Syndrome 4 |
|
FCAS4
|
Nlrc4-Related Familial Cold Autoinflammatory Syndrome
|
|
Nlrc4-Related Familial Cold Urticaria
|
Autoinflammatory, Cold, Familial, Syndrome, Type 4
|
|
|
| Neutrophilic Dermatosis, Acute Febrile |
|
Sweet Syndrome
|
Acute Febrile Neutrophilic Dermatosis
|
|
Ss
|
AFND
|
|
Pyrin-Associated Autoinflammatory Disease
|
PAAND
|
|
Gomm-Button Disease
|
Sweet'S Syndrome
|
|
Gomm Button Disease
|
Sweets Syndrome
|
|
Acromelic Frontonasal Dysostosis
|
Sweet Disease
|
|
|
| Cinca Syndrome |
|
CINCA
|
Nomid
|
|
Cryopyrin-Associated Periodic Syndrome 3
|
Chronic Neurologic Cutaneous And Articular Syndrome
|
|
Multisystem Inflammatory Disease, Neonatal-Onset
|
Caps3
|
|
Chronic Infantile Neurological Cutaneous Articular Syndrome
|
Infantile-Onset Multisystem Inflammatory Disease
|
|
Iomid Syndrome
|
Neonatal-Onset Multisystem Inflammatory Disease
|
|
Nomid Syndrome
|
Prieur-Griscelli Syndrome
|
|
Neonatal Onset Multisystem Inflammatory Disease
|
Chronic Infantile Neurological, Cutaneous And Articular Syndrome
|
|
Iomid
|
Infantile Onset Multisystem Inflammatory Disease
|
|
Prieur Griscelli Syndrome
|
Chronic Infantile Neurological Cutaneous And Articular Syndrome
|
|
Chronic, Infantile, Neurological, Cutaneous, Articular Syndrome
|
Chronic Infantile Neurologic Cutaneous And Articular Syndrome
|
|
Chronic Infantile Neurological, Cutaneous, And Articular Syndrome
|
Cryopyrin-Associated Periodic Syndromes
|
|
|
| Muckle-Wells Syndrome |
|
MWS
|
Urticaria-Deafness-Amyloidosis Syndrome
|
|
Uda Syndrome
|
Neutrophilic Urticaria
|
|
Urticaria, Deafness And Amyloidosis
|
Cryopyrin-Associated Periodic Syndrome 2
|
|
Caps2
|
Muckle Wells Syndrome
|
|
Urticaria-Deafness-Amyloidosis
|
Cryopyrin-Associated Periodic Syndromes
|
|
|
| Retinal Lattice Degeneration |
|
Palisade Degeneration Of Retina
|
Lattice Retinal Degeneration
|
|
|
| Blau Syndrome |
|
Arthrocutaneouveal Granulomatosis
|
Jabs Syndrome
|
|
BLAUS
|
Sarcoidosis, Early-Onset
|
|
Acug
|
Granulomatous Inflammatory Arthritis, Dermatitis, And Uveitis, Familial
|
|
Eos
|
Granulomatosis, Familial Juvenile Systemic
|
|
Granulomatosis, Familial, Blau Type
|
Familial Juvenile Systemic Granulomatosis
|
|
Early Onset Sarcoidosis
|
Synovitis Granulomatous With Uveitis And Cranial Neuropathies
|
|
Early-Onset Sarcoidosis
|
Familial Granulomatosis, Blau Type
|
|
Pediatric Granulomatous Arthritis
|
Familial Granulomatosis Blau Type
|
|
Familial Granulomatous Inflammatory Arthritis Dermatitis And Uveitis
|
Synovitis, Granulomatous, With Uveitis And Cranial Neuropathies
|
|
|
| Pityriasis Rubra Pilaris |
|
PRP
|
Devergie'S Disease
|
|
Prp - [Pityriasis Rubra Pilaris]
|
|
|
| Pustulosis Of Palm And Sole |
|
Psoriasis
|
Acropustulosis
|
|
Palmoplantar Pustulosis
|
Pustular Psoriasis Of The Palms And/Or Soles
|
|
Pustulosis Of Palms And Soles
|
Acrodermatitis Continua Of Hallopeau
|
|
Generalized Pustular Psoriasis
|
|
|
| Familial Behcet-Like Autoinflammatory Syndrome |
|
Autoinflammatory Syndrome, Familial, Behcet-Like
|
A20 Haploinsufficiency
|
|
|
| Inflammatory Bowel Disease |
|
Inflammatory Bowel Diseases
|
Bowel Disease, Inflammatory
|
|
|
| Erysipelas |
|
|
| Autoinflammation, Panniculitis, And Dermatosis Syndrome |
|
Otulipenia
|
Otulin-Related Autoinflammatory Syndrome
|
|
AIPDS
|
Oras
|
|
Infantile-Onset Periodic Fever-Panniculitis-Dermatosis Syndrome
|
Autoinflammation, Panniculitis And Dermatosis Syndrome
|
|
Otulin Deficiency
|
|
|
| Peroxisomal Disease |
|
Peroxisomal Disorder
|
Peroxisomal Disorders
|
|
Peroxisomal Defects
|
|
|
| Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome |
|
Jacobs Syndrome
|
Arthropathy-Camptodactyly Syndrome
|
|
Pericarditis-Arthropathy-Camptodactyly Syndrome
|
Xyy Syndrome
|
|
Pac Syndrome
|
Cacp Syndrome
|
|
CACP
|
Fibrosing Serositis, Familial
|
|
Camptodactyly-Arthropathy-Pericarditis Syndrome
|
Cap Syndrome
|
|
47, Xyy Syndrome
|
47,Xyy Syndrome
|
|
Double Y Syndrome
|
Camptodactyly-Arthropathy-Coxa-Vara-Pericarditis Syndrome
|
|
Hypertrophic Synovitis, Congenital Familial
|
Congenital Familial Hypertrophic Synovitis
|
|
Xyy Karyotype
|
Y Disomy
|
|
Yy Syndrome
|
Familial Fibrosing Serositis
|
|
Disomy Y
|
Double Y
|
|
Camptodactyly Arthropathy Coxa Vara Pericarditis Syndrome
|
Arthropathy Camptodactyly Syndrome
|
|
Camptodactyly Arthropathy Pericarditis Syndrome
|
Pericarditis Arthropathy Camptodactyly Syndrome
|
|
Jacob'S Syndrome
|
47,Xyy
|
|
Cdags Syndrome
|
|
|
