| Diseases |
Alias |
|
| 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
|
|
|
| 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
|
|
|
| Familial Mediterranean Fever, Autosomal Dominant |
|
Familial Mediterranean Fever, Ad
|
Fmf, Autosomal Dominant
|
|
ADFMF
|
Fever, Mediterranean, Familial, Autosomal Dominant
|
|
|
| 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
|
|
|
| Autoinflammatory Syndrome |
|
|
| Motor Stereotypies |
|
|
| Brachydactyly |
|
|
| Stereotypic Movement Disorder |
|
Stereotypy Habit Disorder
|
Stereotyped Repetitive Movements
|
|
Stereotyped Disorder
|
Stereotypes Nos
|
|
Stereotype Habit Disorder
|
|
|
| Cryptorchidism, Unilateral Or Bilateral |
|
Cryptorchidism
|
Undescended Testicle
|
|
Undescended Testis
|
Cryptorchism
|
|
Undescended Testicles
|
CRYPTO
|
|
Impaired Testicular Descent
|
Cryptosporidiosis
|
|
Retained Testis
|
Unilateral Cryptorchidism
|
|
Unilateral Undescended Testis
|
Nondescent Unilateral Testicle
|
|
Unilateral Cryptorchism
|
Ectopic Testis, Unilateral
|
|
Bilateral Cryptorchidism
|
Bilateral Cryptorchism
|
|
Bilateral Nondescent Testicle
|
Bilateral Undescended Testes
|
|
Bilateral Ectopic Testes
|
|
|
| Microcephaly |
|
Microencephaly
|
Microcephalus
|
|
Microcephalic
|
Nanocephaly
|
|
Congenital Microcephaly
|
Brain Hypoplasia
|
|
Brain Nondevelopment
|
Cephalic Hypoplasia
|
|
Undeveloped Cerebrum
|
Undeveloped Brain
|
|
Micrencephalon
|
Micrencephaly
|
|
|
| Hereditary Periodic Fever Syndrome |
|
Hereditary Periodic Fever Syndromes
|
|
|
| Intermittent Hydrarthrosis |
|
Intermittent Joint Effusion
|
Hydrops Articulorum Intermittens
|
|
|
| Pyoderma Gangrenosum |
|
Phagedenic Pyoderma
|
Phagedena Geometric
|
|
|
| Vasculitis |
|
Angiitis
|
Autoimmune Vasculitis
|
|
Systemic Vasculitis
|
Vasculitis, Autoimmune
|
|
|
| Brucellosis |
|
Mediterranean Fever
|
Malta Fever
|
|
Undulant Fever
|
Gibraltar Fever
|
|
Bang'S Disease
|
Maltese Fever
|
|
Cyprus Fever
|
Rock Fever
|
|
Brucellosis Infection
|
Brucella Infection
|
|
|
| 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
|
|
|
| Pyoderma |
|
|
| Pericarditis |
|
|
| Henoch-Schoenlein Purpura |
|
Henoch-Schonlein Purpura
|
Iga Vasculitis
|
|
Allergic Purpura
|
Anaphylactoid Purpura
|
|
Rheumatoid Purpura
|
Immunoglobulin A Vasculitis
|
|
Vascular Purpura
|
Purpura Rheumatica
|
|
Henoch-Schönlein Purpura
|
Autoimmune Purpura
|
|
Henoch-Schnlein Purpura
|
Henoch-Sch@Nlein Purpura
|
|
Henoch-Scholein Purpura
|
Purpura, Autoimmune
|
|
Henoch Schonlein Purpura
|
Immunoglobulin-A Vasculitis
|
|
Purpura, Schonlein-Henoch
|
Purpura, Schönlein-Henoch
|
|
Hsp -
|
Schönlein-Henoch Purpura
|
|
|
| Hydrarthrosis |
|
|
| Polyarteritis Nodosa |
|
Polyarteritis
|
Periarteritis Nodosa
|
|
Pan
|
Periarteritis
|
|
Kussmaul-Maier Disease
|
Panarteritis Nodosa
|
|
Kussmaul Disease
|
Pan - [Polyarteritis Nodosa]
|
|
Polyangiitis
|
Panangiitis
|
|
Arteritis Nodosa
|
|
|
| Amyloidosis |
|
Amyloid Disease
|
Amyloid
|
|
Amyloid Degeneration
|
Amyloidosis Nos
|
|
Amyloid Deposition
|
Amyloid Infiltration
|
|
Idiopathic Amyloidosis
|
Hyaloid Degeneration
|
|
Lardaceous Degeneration
|
|
|
| Serum Amyloid A Amyloidosis |
|
Aa Amyloidosis
|
Secondary Amyloidosis
|
|
Reactive Systemic Amyloidosis
|
Apo Serum Amyloid A Amyloidosis
|
|
Inflammation Aa Amyloidosis
|
Amyloidosis Aa
|
|
Amyloid A Amyloidosis
|
Inflammatory Amyloidosis
|
|
Reactive Amyloidosis
|
Amyloidosis Secondary
|
|
Secondary Systemic Amyloidosis
|
Amyloid Aa
|
|
|
| Pleurisy |
|
|
| 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
|
|
|
| Relapsing Fever |
|
Febris Recurrens
|
Novy Febris Recurrens
|
|
Novy Relapsing Fever
|
|
|
| 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
|
|
|
| Gout |
|
Gouty Arthritis
|
Articular Gout
|
|
Gouty Arthropathy
|
Arthritis, Gouty
|
|
Arthritis Gouty
|
Idiopathic Gout
|
|
Idiopathic Gout, Unspecified Site
|
Gouty Bursitis
|
|
Uratic Arthritis
|
Gout Nos
|
|
Gouty
|
Gouty Diathesis
|
|
|
| Pharyngitis |
|
Acute Pharyngitis
|
Chronic Pharyngitis
|
|
Acute Sore Throat
|
Chronic Sore Throat
|
|
Persistent Sore Throat
|
Pharyngeal Diseases
|
|
Chronic Pharyn/Nasopharyngitis
|
Chronic Pharyngitis And Nasopharyngitis
|
|
Inflamed Throat
|
Pharyngeal Disease
|
|
Pharyngeal Disorder
|
Pharyngitis - Acute
|
|
Sore Throat - Chronic
|
Acute Pharyngitis Nos
|
|
Acute Sore Throat Nos
|
Acute Throat Inflammation
|
|
Infective Pharyngitis
|
Infection Of Pharynx
|
|
Acute Infective Pharyngitis
|
Acute Infective Pharyngitis Nos
|
|
Acute Pharyngeal Inflammation
|
Inflammation Of The Throat
|
|
Throat Inflammation
|
Throat Infection
|
|
Putrid Pharyngitis
|
Pharyngeal Inflammation
|
|
Pharyngitis Nos
|
Chronic Throat Pain
|
|
Throat Catarrh
|
|
|
| Kidney Disease |
|
Renal Failure
|
Kidney Failure
|
|
Kidney Diseases
|
Nephropathy
|
|
Abnormality Of The Kidney
|
Impaired Renal Function Disease
|
|
Renal Anomaly
|
Kidney Dysfunction
|
|
Renal Disease
|
Nephropathies
|
|
Renal Failure Adverse Event
|
Abnormal Renal Function
|
|
|
| Heart Disease |
|
Heart Failure
|
Congenital Heart Disease
|
|
Heart Diseases
|
Congenital Heart Defects
|
|
Congenital Heart Defect
|
Heart Malformation
|
|
Congenital Anomaly Of Heart
|
Heart Defect
|
|
Heart-Congenital Defect
|
Congenital Heart Disorder
|
|
Heart Defects Congenital
|
Heart Defects, Congenital
|
|
Heart Defects
|
Heart Disease, Congenital
|
|
Disease, Heart, Congenital
|
Congestive Heart Failure
|
|
|
| Palindromic Rheumatism |
|
Hench'S Syndrome
|
Hench-Rosenberg Syndrome
|
|
Palindromic Rheumatism Syndrome
|
Palindromic Arthritis
|
|
|
| Familial Cold Autoinflammatory Syndrome 1 |
|
Cold Hypersensitivity
|
Cold-Induced Autoinflammatory Syndrome, Familial
|
|
FCAS1
|
Fcas
|
|
Fcu
|
Cryopyrin-Associated Periodic Syndrome 1
|
|
Caps1
|
Familial Cold Urticaria
|
|
Cold Urticaria, Familial
|
Familial Cold Inflammatory Syndrome 1
|
|
Familial Cold-Induced Autoinflammatory Syndrome
|
Autoinflammatory Syndrome, Cold, Familial, Type 1
|
|
|
| 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
|
|
|
| Erysipeloid |
|
Infection Due To Erysipelothrix Rhusiopathiae
|
Erysipelothrix Infection
|
|
|
| Arthritis |
|
Inflammatory Joint Disease
|
Inflammatory Disorder Of Joint
|
|
|
| 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
|
|
|
| Proteasome-Associated Autoinflammatory Syndrome 1 |
|
Jmp Syndrome
|
Nakajo-Nishimura Syndrome
|
|
Nkjo
|
Autoinflammation, Lipodystrophy, And Dermatosis Syndrome
|
|
Proteasome-Associated Autoinflammatory Syndrome 1 And Digenic Forms
|
Nakajo Syndrome
|
|
PRAAS1
|
Chronic Atypical Neutrophilic Dermatosis With Lipodystrophy And Elevated Temperature Syndrome
|
|
Candle
|
Joint Contractures, Muscular Atrophy, Microcytic Anemia, And Panniculitis-Induced Lipodystrophy
|
|
Aldd
|
Inflammation
|
|
Joint Contractures - Muscle Atrophy - Microcytic Anemia - Panniculitis-Induced Lipodystrophy
|
Nakajo Nishimura Syndrome
|
|
Amyotrophy Fat Tissue Anomaly
|
Japanese Autoinflammatory Syndrome With Lipodystrophy
|
|
Jasl
|
Joint Contractures Muscular Atrophy Microcytic Anemia And Panniculitis-Induced Lipodystrophy
|
|
Nns
|
Nodular Erythema With Digital Changes
|
|
Secondary Hypertrophic Osteoperiostosis With Pernio
|
|
|
| Cervical Adenitis |
|
|
| Hidradenitis |
|
|
| Hidradenitis Suppurativa |
|
Acne Inversa
|
Suppurative Hidradenitis
|
|
Acne Inversa, Familial
|
Apocrinitis
|
|
Hidradenitides, Suppurative
|
Hidradenitis, Suppurative
|
|
Suppurative Hidradenitides
|
Inverse Acne
|
|
|
| Amyloidosis, Familial Visceral |
|
Ostertag Type Amyloidosis
|
German Type Amyloidosis
|
|
Familial Renal Amyloidosis
|
Amyloidosis Viii
|
|
Amyloidosis, 3 Or More Types
|
Familial Visceral Amyloidosis
|
|
Familial Amyloid Nephropathy
|
Hereditary Amyloid Nephropathy
|
|
Amyloidosis, Familial Renal
|
Amyloidosis, Systemic Nonneuropathic
|
|
Amyloidosis Familial Visceral
|
Amyloidosis 8
|
|
Amyloidosis, Ostertag Type
|
Hereditary Amyloidosis With Primary Renal Involvement
|
|
Hereditary Renal Amyloidosis
|
Renal Amyloidosis
|
|
Amyloidosis, Renal
|
Systemic Nonneuropathic Amyloidosis
|
|
Amyloidosis Familial Renal
|
Amyloidosis Systemic Nonneuropathic
|
|
Hereditary Amyloidosis With Primary Renal Involement
|
AMYL8
|
|
Systemic Non-Neuropathic Amyloidosis
|
Amyloid Nephropathy
|
|
|
| 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
|
|
|
| Familial Cold Autoinflammatory Syndrome |
|
Familial Cold Urticaria
|
Fcas
|
|
Familial Polymorphous Cold Eruption
|
Fcu
|
|
Cold Hypersensitivity
|
|
|
| Submandibular Adenitis |
|
Submandibular Lymphadenitis
|
|
|
| Erysipelas |
|
|
| Aphthous Stomatitis |
|
Oral Ulcer
|
Canker Sore
|
|
Aphtha
|
Aphthous Ulceration
|
|
Oral Aphthae
|
Oral Aphthous Ulcer
|
|
Canker Sores
|
Stomatitis, Aphthous
|
|
Minor Oral Aphthous Ulceration
|
|
|
| Peritonitis |
|
Retractile Mesenteritis
|
Sclerosing Mesenteritis
|
|
Acute Generalized Peritonitis
|
Primary Bacterial Peritonitis
|
|
Idiopathic Sclerosing Mesenteritis
|
Mesenteric Panniculitis
|
|
Peritoneal Retractile Mesenteritis
|
Liposclerotic Mesenteritis
|
|
Mesenteric Fibromatosis
|
Mesenteric Lipodystrophy
|
|
Mesenteric Lipogranuloma
|
Fibromatosis, Abdominal
|
|
Peritoneum Inflammation
|
Peritonitis Of Undetermined Cause
|
|
Peritonitis Of Unspecified Cause
|
Pelviperitonitis
|
|
Pelvic Peritonitis, Nos
|
Generalised Peritonitis Nos
|
|
Abdominal Peritonitis
|
Acute Idiopathic Peritonitis
|
|
Acute Lesser Sac Peritonitis
|
Acute Peritoneal Inflammation
|
|
Diffuse Peritonitis
|
Peritoneal Inflammation
|
|
Acute Primary Peritonitis
|
Pneumococcal Peritonitis
|
|
|
| Stomatitis |
|
|
| Acne |
|
Acne Vulgaris
|
Acne Varioliformis
|
|
Frontalis Acne
|
|
|
| Osteomyelitis |
|
|
| Conjunctivitis |
|
Madras Eye
|
Adenoviral Conjunctivitis
|
|
Acute Adenoviral Follicular Conjunctivitis
|
Inclusion Conjunctivitis Of The Adult
|
|
Swimming-Pool Conjunctivitis
|
Inflammation Of Conjunctiva
|
|
Ophthalmia
|
Acute Conjunctivitis
|
|
Eye Catarrh
|
Catarrhal Ophthalmia
|
|
Koch-Weeks Conjunctivitis
|
|
|
| Hypersensitivity Vasculitis |
|
Cutaneous Small Vessel Vasculitis
|
Hypersensitivity Angiitis
|
|
Cutaneous Leukocytoclastic Vasculitis
|
Leukocytoclastic Angiitis
|
|
Vasculitis, Leukocytoclastic, Cutaneous
|
Leukocytoclastic Vasculitis
|
|
Cutaneous Leukocytoclastic Angiitis
|
Cutaneous Hypersensitivity Vasculitis
|
|
Vasculitis Hypersensitivity
|
Drug Induced Cutaneous Vasculitis
|
|
Allergic Vasculitis
|
|
|
| Myelitis |
|
Spinal Cord Inflammation Nos
|
Radiculomyelitis Nos
|
|
Myeloradiculitis
|
|
|
| Familial Cold Autoinflammatory Syndrome 2 |
|
FCAS2
|
Nlrp12-Associated Hereditary Periodic Fever Syndrome
|
|
Familial Cold Autoinflammatory Syndrome Type 2
|
Familial Cold-Induced Autoinflammatory Syndrome Type 2
|
|
Naps12
|
Familial Cold Autoinflammatory Syndrome 2, Susceptibility To
|
|
Autoinflammatory Syndrome, Cold, Familial, Type 2
|
|
|
| Nail-Patella Syndrome |
|
Turner-Kieser Syndrome
|
Onychoosteodysplasia
|
|
Fong Disease
|
NPS
|
|
Hereditary Onycho-Osteodysplasia
|
Nps1
|
|
Hereditary Onychoostedysplasia
|
Iliac Horn Syndrome
|
|
Nail Patella Syndrome
|
Turner-Kiser Syndrome
|
|
Arthro-Onychodysplasia
|
Nps 1
|
|
Osteo-Onychodysplasia
|
Hereditary Osteo-Onychodysplasia
|
|
Osterreicher Syndrome
|
Pelvic Horn Syndrome
|
|
Österreicher-Turner Syndrome
|
Nps - [Nail-Patella Syndrome]
|
|
Hood - [Hereditary Onycho-Osteodysplasia] Syndrome
|
|
|
| Hypersensitivity Reaction Type Iii Disease |
|
Immune Complex Diseases
|
Immune Complex Disease
|
|
Type Iii Hypersensitivity Reaction Disease
|
|
|
| Familial Behcet-Like Autoinflammatory Syndrome |
|
Autoinflammatory Syndrome, Familial, Behcet-Like
|
A20 Haploinsufficiency
|
|
|
| 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
|
|
|
| Adult-Onset Still'S Disease |
|
Adult-Onset Still Disease
|
Adult Onset Still'S Disease
|
|
Adult Still'S Disease
|
Still'S Disease Adult Onset
|
|
Aosd
|
Wissler-Fanconi Syndrome
|
|
Stills Disease Adult-Onset
|
Still'S Disease, Adult-Onset
|
|
Wissler'S Syndrome
|
|
|
| Sebaceous Gland Disease |
|
Sebaceous Gland Anomaly
|
Sebaceous Gland Diseases
|
|
|
| Aseptic Meningitis |
|
Acute Aseptic Meningitis
|
Meningitis Aseptic
|
|
Meningitis, Aseptic
|
|
|
| Schnitzler Syndrome |
|
Chronic Urticaria With Gammopathy
|
Chronic Urticaria With Macroglobulinemia
|
|
Chronic Urticaria With Gammapathy
|
|
|
| Peroxisomal Disease |
|
Peroxisomal Disorder
|
Peroxisomal Disorders
|
|
Peroxisomal Defects
|
|
|
| Autoimmune Disease Of Cardiovascular System |
|
|
| Pericardium Disease |
|
|
| Iga Glomerulonephritis |
|
Iga Nephropathy
|
Glomerulonephritis, Iga
|
|
Berger'S Iga Or Igg Nephropathy
|
Focal Glomerulonephritis
|
|
Primary Iga Nephropathy
|
Segmental Glomerulonephritis
|
|
Berger Disease
|
Berger'S Disease
|
|
Igan
|
Nephritis, Iga Type
|
|
Nephropathy Iga
|
Glomerulonephritis Focal
|
|
Iga Nephropathy, Susceptibility To
|
Primary Immunoglobulin A Nephropathy
|
|
|
| Chronic Meningitis |
|
|
| Chondrocalcinosis |
|
Pseudogout
|
Calcium Pyrophosphate Deposition Disease
|
|
Familial Chondrocalcinosis
|
Chondrocalcinosis Nos
|
|
Cppd - [Calcium Pyrophosphate Deposition Disease]
|
Cpdd - [Calcium Pyrophosphate Deposition Disease]
|
|
Chondrocalcinosis, Due To Pyrophosphate Crystals, Involving Unspecified Site
|
Chondrocalcinosis, Cause Unspecified
|
|
Chondrocalcinosis Due To Pyrophosphate Crystals
|
Chondrocalcinosis Articularis
|
|
Calcium Pyrophosphate Arthritis And Periarthritis
|
|
|
| Lymph Node Disease |
|
Abnormality Of The Lymph Nodes
|
Disorder Of Lymph Node
|
|
|
| Rheumatoid Arthritis |
|
RA
|
Arthritis, Rheumatoid
|
|
Rheumatoid Arthritis, Susceptibility To
|
Arthritis Or Polyarthritis, Rheumatic
|
|
Atrophic Arthritis
|
Rheumatism Arthritis
|
|
Rheumatoid Polyarthritis
|
|
|
| Primary Bacterial Infectious Disease |
|
|
| Spondyloarthropathy |
|
Spondylarthropathies
|
Spondarthropathy
|
|
Spondylarthrosis
|
Spondyloarthropathy, Susceptibility To
|
|
Spondylarthritis
|
|
|
| Systemic Lupus Erythematosus |
|
Lupus Nephritis
|
SLE
|
|
Disseminated Lupus Erythematosus
|
Systemic Lupus Erythematosus, Susceptibility To
|
|
Lupus Erythematosus, Systemic
|
Lupus Nephritis, Susceptibility To
|
|
Libman-Sacks Disease
|
Systemic Lupus Erythematosus Susceptibility To
|
|
Sle - Lupus Erythematosus, Systemic
|
Le Syndrome
|
|
Lupus
|
Lupus Erythematosus Systemic
|
|
Lupus Erythematosus, Systemic, Susceptibility To
|
Lupus Vulgaris
|
|
Lupus Erythematosus, Discoid
|
Lupus Erythematosus
|
|
Systemic Lupus Erythematosus Nos
|
Sle - [Systemic Lupus Erythematosus]
|
|
|
| Gestational Trophoblastic Neoplasm |
|
Hydatidiform Mole
|
Molar Pregnancy
|
|
Gestational Trophoblastic Neoplasia
|
Gestational Trophoblastic Tumor
|
|
Gtn
|
Gestational Trophoblastic Disease
|
|
Gestational Trophoblastic Neoplasms
|
Hydatidiform Mole, Recurrent, 1
|
|
Hydatidiform Mole Benign
|
Trophoblastic Disease
|
|
Trophoblastic Disease Nos
|
Trophoblastic Disorder
|
|
Vesicular Mole Nos
|
Vesicular Mole
|
|
Hydatidiform Mole Nos
|
|
|
| Aicardi-Goutieres Syndrome |
|
Aicardi Goutieres Syndrome
|
Cree Encephalitis
|
|
Aicardi-Goutières Syndrome
|
Encephalopathy With Basal Ganglia Calcification
|
|
Ags
|
Encephalopathy With Intracranial Calcification And Chronic Lymphocytosis Of Cerebrospinal Fluid
|
|
Pseudotoxoplasmosis Syndrome
|
Encephalopathy, Familial Infantile, With Calcification Of Basal Ganglia And Chronic Cerebrospinal Fluid Lymphocytosis
|
|
Familial Infantile Encephalopathy With Intracranial Calcification And Chronic Cerebrospinal Fluid Lymphocytosis
|
Aicardi-Goutieres Syndrome 1
|
|
|
| Lipoprotein Quantitative Trait Locus |
|
Coronary Artery Disease
|
Coronary Artery Anomaly
|
|
Coronary Artery Disease, Susceptibility To
|
Myocardial Ischemia
|
|
Congenital Anomaly Of Coronary Artery
|
Coronary Arteriosclerosis
|
|
Coronary Disease
|
Coronary Heart Disease
|
|
Coronary Artery Disorder
|
LPAQTL
|
|
Lpa Deficiency, Congenital
|
Coronary Artery Abnormality
|
|
Coronary Artery Anomaly, Congenital
|
Chd
|
|
Coronary Syndrome
|
Congenital Malformations Of Coronary Vessels
|
|
Malformation Of Coronary Vessels
|
Congenital Coronary Artery Anomaly
|
|
Congenital Coronary Artery Deformity
|
Congenital Coronary Artery Disorder
|
|
Abnormal Coronary Artery
|
Congenital Coronary Artery Malposition
|
|
Congenital Coronary Disease
|
Congenital Anomaly Of Coronary Arteries
|
|
|
| Skin Disease |
|
Skin Diseases
|
Genodermatosis
|
|
Abnormality Of The Skin
|
Skin Diseases, Genetic
|
|
Skin And Subcutaneous Tissue Disease
|
Dermatologic Disorders
|
|
|
