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Master List of Awareness Causes - I | Personalized Cause

Comprehensive master list of every awareness cause beginning with the letter I and the corresponding awareness ribbon color.

Master List of Awareness Causes and Associated Colors

All Causes Beginning with the Letter I:


I Cell Disease

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

I Cell Disease is also known as:
• Inclusion Cell Disease
• Leroy Disease
• ML Disorder, Type II
• ML II
• Mucolipidosis II
• N-Acetylglucosamine-1-Phosphotransferase Deficiency

What is I Cell Disease?
I-Cell Disease (Mucolipidosis II) is a rare inherited metabolic disorder characterized by coarse facial features, skeletal abnormalities and mental retardation. This disorder belongs to a group of diseases known as lysosomal storage disorders. Lysosomes are particles bound in membranes within cells that break down certain fats and carbohydrates.

Categories

• Congenital and Genetic Diseases
• Metabolic Disorders
• Musculoskeletal Diseases

Cause Classification: Medical


Ichthyosis

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Ichthyosis is also known as:
• Disorders of Cornification

Subdivisions of Ichthyosis
• Chanarin-Dorfman Syndrome (Neutral Lipid Storage Disease)
• CHILD Syndrome (Unilateral Hemidysplasia)
• Congenital Ichthyosiform Erythroderma (CIE) • Conradi-Hunermann Syndrome (X-Linked Dominant Chondrodysplasia Punctata)
• Darier Disease
• Epidermal Nevi (Ichthyosis Hystrix, Linear Epidermal Nevus)
• Epidermolytic Hyperkeratosis (EHK)
• Erythrokeratodermia Variabilis (EKV)
• Giroux-Barbeau Syndrome
• Hailey-Hailey Disease (Benign Familial Pemphigus)
• Harlequin Ichthyosis (Harlequin Fetus)
• Ichthyosis Hystrix Curth-Macklin Type
• Ichthyosis Vulgaris (Ichthyosis Simplex)
• Keratosis Follicularis Spinulosa Decalvans
• KID Syndrome (Keratitis, Ichthyosis, Deafness)
• Lamellar Ichthyosis
• Multiple Sulfatase Deficiency
• Netherton Syndrome (Ichthyosis Linearis Circumflexa)
• Pachyonychia Congenita
• Palmoplantar Keratodermas (PPK)
• Peeling Skin Syndrome
• Pityriasis Rubra Pilaris (PRP)
• Refsum's Disease (Phytanic Acid Storage Disease)
• Rud's Syndrome
• Sjogren-Larsson Syndrome
• Tay's Syndrome (Trichothiodystrophy, IBIDS Syndrome)
• X-Linked Ichthyosis

What is Ichthyosis?
Ichthyosis is a general term for a family of rare genetic skin diseases characterized by dry, thickened, scaling skin. The various forms are distinguished from one another by the extent of the scaling and how widely and where the scaling is scattered over the body; the presence or absence and intensity of reddening of the skin; 3) the mode of inheritance; and 4) the character of associated abnormalities.

Categories

• Skin Diseases

Cause Classification: Medical


Ichthyosis Hystrix, Curth Macklin Type

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Ichthyosis Hystrix, Curth Macklin Type is also known as:
• Disorder of Cornification 8, Curth-Macklin Type
• DOC 8, Curth-Macklin Type

What is Ichthyosis Hystrix, Curth Macklin Type?
Ichthyosis Hystrix, Curth-Macklin Type is a rare inherited skin disorder. It is characterized by scaling skin (ichthyosis) ranging from mild to severe. The patches of scaly, thickened skin range from spotty to severe, and may appear on almost any part of the body.

Categories

• Congenital and Genetic Diseases
• Skin Diseases

Cause Classification: Medical


Ichthyosis Vulgaris

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Ichthyosis Vulgaris is also known as:
• Ichthyosis Simplex

What is Ichthyosis Vulgaris?
In Ichthyosis Vulgaris, the skin cells are produced at a normal rate, but they do not shed normally at the surface of the outermost layer of skin and are not shed as quickly as they should be. The result is a build-up of scales. Fine scales usually develop on the back and over muscles near the joints, such as an elbow or knee. Ichthyosis is usually most common and severe over the lower legs.

Categories

• Skin Diseases

Cause Classification: Medical


Ichthyosis, CHILD Syndrome

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Ichthyosis, CHILD Syndrome is also known as:
• CHILD Naevus
• CHILD Nevus
• Congenital Hemidysplasia with Ichthyosis Erythroderma and Limb Defects
• Disorders of Cornification 16
• DOC 16, Unilateral Hemidysplasia Type
• Unilateral Hemidysplasia Type
• Unilateral Ichthyosiform Erythroderma with Ipsilateral Malformations, Limb

What is Ichthyosis, CHILD Syndrome?
CHILD Syndrome (an acronym for Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects) is an inherited disorder, affecting primarily women, that is characterized by ichthyosis-like skin abnormalities and limb defects on one side of the body.

Categories

• Congenital and Genetic Diseases
• Skin Diseases

Cause Classification: Medical


Ichthyosis, Erythrokeratodermia Variabilis

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Ichthyosis, Erythrokeratodermia Variabilis is also known as:
• EKV • Keratosis Rubra Figurata
• Mendes Da Costa Syndrome

What is Ichthyosis, Erythrokeratodermia Variabilis?
Erythrokeratodermia Variabilis is an inherited skin disorder characterized by two features: short-lasting red patches in various sizes and shapes that may involve any part of the body; and thickening of the skin (hyperkeratosis). The hyperkeratosis can either be generalized, or localized as fixed, sharply defined, thickened plaques. The hyperkeratosis may also involve the skin of the palms and soles. Skin lesions are made worse by sudden changes in temperature and friction. The red patches may be accompanied by a burning sensation.

Categories

• Skin Diseases

Cause Classification: Medical


Ichthyosis, Erythrokeratolysis Hiemalis

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Ichthyosis, Erythrokeratolysis Hiemalis is also known as:
• Disorder of Cornification 19 (Erythrokeratolysis Hiemalis)
• DOC 19
• Erythrokeratolysis Hiemalis
• Keratolytic Winter Erythema
• Oudtshoorn Skin

What is Ichthyosis, Erythrokeratolysis Hiemalis?
Erythrokeratolysis Hiemalis is an extremely rare form of ichthyosis that was first described in South Africa but has subsequently been identified in other countries. The disorder is characterized by periodic attacks of red plaques that are distributed equally on both sides of the body.

Category

• Skin Diseases

Cause Classification: Medical


Ichthyosis, Harlequin Type

Awareness Ribbon Color:

Blue Jeans Ribbon for Genetic Diseases

Ichthyosis, Harlequin Type is also known as:
• Harlequin Fetus
• Ichthyosis Fetalis

What is Ichthyosis, Harlequin Type?
Harlequin Ichthyosis is a rare genetic skin disorder. The newborn infant is covered with plates of thick skin that crack and split apart. The thick plates can pull at and distort facial features and can restrict breathing and eating. Harlequin infants need to be cared for in the neonatal intensive care unit immediately. Harlequin Ichthyosis is inherited as an autosomal recessive trait.

Categories

• Congenital and Genetic Diseases
• Skin Diseases

Cause Classification: Medical


Ichthyosis, Keratosis Follicularis Spinulosa Decalvans

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Ichthyosis, Keratosis Follicularis Spinulosa Decalvans is also known as:
• Disorder of Cornification 24
• DOC 24
• Siemens Syndrome

What is Ichthyosis, Keratosis Follicularis Spinulosa Decalvans?
Keratosis Follicularis Spinulosa Decalvans (KFSD) is a rare, inherited, skin disorder that affects men predominately and is characterized by hardening of the skin (keratosis) in several parts of the body.

Categories

• Congenital and Genetic Diseases
• Eye Diseases
• Skin Diseases

Cause Classification: Medical


Ichthyosis, Lamellar

Awareness Ribbon Color:

Blue Jeans Ribbon for Genetic Diseases

Ichthyosis, Lamellar is also known as:
• Collodion Baby
• Ichthyosis Congenita
• Lamellar Ichthyosis, Type 1 and Type 2
• Non-Bullous Congenital Ichthyosiform Erythroderma (Non-Bullous CIE)

What is Ichthyosis, Lamellar?
Lamellar Ichthyosis is a rare genetic skin disorder. In Lamellar Ichthyosis, the skin cells are produced at a normal rate, but they do not separate normally at the surface of the outermost layer of skin and are not shed as quickly as they should be. The result of this retention is the formation of scales.

Categories

• Congenital and Genetic Diseases
• Eye Diseases
• Skin Diseases

Cause Classification: Medical


Ichthyosis, Netherton Syndrome

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Ichthyosis, Netherton Syndrome is also known as:
• Comel-Netherton Syndrome
• Ichthyosis Linearis Circumflexa

What is Ichthyosis, Netherton Syndrome?
Netherton Syndrome is a rare hereditary disorder characterized by scaling skin, hair anomalies, increased susceptibility to atopic eczema, elevated IgE levels, and other related symptoms. Netherton Syndrome is inherited as an autosomal recessive trait.

Categories

• Congenital and Genetic Diseases
• Eye Diseases
• Immune System Diseases
• Skin Diseases

Cause Classification: Medical


Ichthyosis, Trichothiodystrophy

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

IIchthyosis, Trichothiodystrophy is also known as:
• IBIDS Syndrome
• PIBIDS Syndrome
• Tay Syndrome
• TTD

What is Ichthyosis, Trichothiodystrophy?
Trichothiodystrophy is a hereditary disorder characterized by brittle hair, which may be accompanied by a variety of other manifestations. It is sometimes called PIBIDS, a term that refers to the association of Photosensitivity Ichthyosis, Brittle hair, Intellectual Impairment, Decreased Fertility, and Short Stature. Without photosensitivity the condition has been termed IBIDS, and without ichthyosis, BIDS.

Categories

• Congenital and Genetic Diseases
• Male Reproductive Diseases
• Skin Diseases

Cause Classification: Medical


Ichthyosis, X Linked

Awareness Ribbon Color:

Blue Jeans Ribbon for Genetic Diseases

Ichthyosis, X Linked is also known as:
• Placental Steroid Sulfatase Deficiency; STS
• Recessive X-linked Ichthyosis
• Steroid Sulfatase Deficiency
• Steroid Sulfatase Deficiency Disease; SSDD

What is Ichthyosis, X Linked?
X-Linked Ichthyosis is a genetic skin disorder that affects males. It is an inborn error of metabolism characterized by a deficiency of the enzyme steroid sulfatase. Under normal conditions, this enzyme breaks down (metabolizes) cholesterol sulfate, a member of the chemical family of steroids. Cholesterol sulfate plays a role in maintaining the integrity of the skin. If steroid metabolism is interrupted and cholesterol sulfate accumulates in the skin cells, the skin cells stick together more strongly than usual. The normal shedding of dead skin cells is inhibited and the skin cells build up and clump into scales.

Categories

• Congenital and Genetic Diseases
• Eye Diseases
• Skin Diseases

Cause Classification: Medical


Idiopathic Inflammatory-Demyelinating Diseases

Awareness Ribbon Color:

Orange Ribbon for Idiopathic Inflammatory-Demyelinating Diseases

What is Idiopathic Inflammatory-Demyelinating Diseases?
Idiopathic Inflammatory-Demyelinating Diseases (IIDDs) include a broad spectrum of central nervous system disorders that can usually be differentiated on the basis of clinical, imaging, laboratory and pathological findings. However, there can be a considerable overlap between at least some of these disorders, leading to misdiagnoses or diagnostic uncertainty. The relapsing-remitting and secondary progressive forms of multiple sclerosis (MS) are the most common IIDDs. Other MS phenotypes include those with a progressive course from onset or with a benign course continuing for years after onset (benign MS).

Categories

• Nervous System Diseases

Cause Classification: Medical


Idiopathic Intracranial Hypertension

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Idiopathic Intracranial Hypertension is also known as:
• Benign Intracranial Hypertension
• Pseudotumor Cerebri

What is Idiopathic Intracranial Hypertension?
Intracranial Hypertension (IH) is characterized by increased pressure inside the skull. Intracranial Hypertension means that the pressure of the fluid that surrounds the brain is too high. Elevated CSF pressure can cause two problems, severe headache and visual loss. If the elevated CSF pressure remains untreated, permanent visual loss or blindness may result. Pseudotumor Cerebri and Benign Intracranial Hypertension are both former names for IH, which are now considered inaccurate.

Categories

• Nervous System Diseases

Cause Classification: Medical


Idiopathic Neonatal Hepatitis

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Idiopathic Neonatal Hepatitis is also known as:
• Idiopathic Neonatal Hepatitis Syndrome
• INH
• Neonatal Giant Cell Hepatitis
• Neonatal Cholestasis

What is Idiopathic Neonatal Hepatitis?
"Neonatal hepatitis" is a somewhat imprecise, general term traditionally used to denote injury to the liver that occurs shortly after birth. Neonatal Cholestasis may be caused by viruses, metabolic disease or genetic disorders, as well as other rare diseases that affect or impair the function of the liver. In some children, the cause of liver injury is unknown.

Categories

• Congenital and Genetic Diseases

Cause Classification: Medical


Idiopathic Pulmonary Fibrosis

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Idiopathic Pulmonary Fibrosis is also known as:
• Cryptogenic Fibrosing Alveolitis
• Idiopathic Diffuse Interstitial Pulmonary Fibrosis
• IPF

What is Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis (IPF) is a chronic lung disorder characterized by thickening, stiffening and scarring of tissue within the lungs. Affected individuals develop shortness of breath and progressive lung disease. Ultimately, IPF results in life-threatening complications such as respiratory failure.

Categories

• Lung Diseases

Cause Classification: Medical


Idiopathic Subglottic Stenosis

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Idiopathic Subglottic Stenosis is also known as:
• Idiopathic Subglottic and Tracheal Stenosis
• iSGS
• ISS

What is Idiopathic Subglottic Stenosis?
Idiopathic Subglottic Stenosis (iSGS) is a narrowing of a specific portion of the windpipe, known as the subglottis. Most patients have scar tissue and inflammation in the affected area.

Categories

• Idiopathic Subglottic Stenosis

Cause Classification: Medical


IgA Nephropathy

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

IgA Nephropathy is also known as:
• Berger's Disease
• Idiopathic Renal Hematuria
• Mesangial IGA Nephropathy

What is IgA Nephropathy?
A nephropathy is a chronic kidney disease that usually first appears during adolescence and young adulthood and often progresses to kidney failure. It usually follows a viral infection of the upper respiratory or gastrointestinal tracts. The major symptom is the passing of blood in the urine.

Categories

• Kidney and Urinary Diseases

Cause Classification: Medical


Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

What is IgG4-Related Sclerosing Disease?
Immunoglobulin G4-Related Disease (IgG4-RD) is an increasingly recognized immune-mediated condition comprised of a collection of disorders that share particular pathologic, serologic, and clinical features. These disorders were previously thought to be unrelated. The commonly shared features include tumor-like swelling of involved organs, a lymphoplasmacytic infiltrate enriched in IgG4-positive plasma cells, and a variable degree of fibrosis that has a characteristic "storiform" pattern. In addition, elevated serum concentrations of IgG4 are found in 60 to 70 percent of patients with IgG4-RD.

Categories

• Immune System Diseases

Cause Classification: Medical


Immune Thrombocytopenia

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Immune Thrombocytopenia is also known as:
• Autoimmune Thrombocytopenic Purpura
• ITP
• Primary Thrombocytopenic Purpura
• Primary Immune Thrombocytopenia

What is Immune Thrombocytopenia?
Immune Thrombocytopenia (ITP) is an autoimmune bleeding disorder characterized by abnormally low levels of blood cells called platelets, otherwise referred to as thrombocytopenia. Platelets are specialized blood cells that maintain the integrity of the blood vessel walls and help prevent and stop bleeding by accelerating clotting. A normal platelet count ranges from approximately 150,000 to 400,000 per microliter of blood depending on the laboratory. If someone has a platelet count lower than 100,000 per microliter of blood with no other reason for low platelets, that person has thrombocytopenia and might have ITP. There is currently no definitive laboratory test to diagnose ITP. Rather ITP is considered a diagnosis of exclusion, meaning that other causes have been excluded or are unlikely. As the platelet count falls, the risk of developing bleeding symptoms increases.

Categories

• Autoimmune Diseases
• Autoinflammatory Diseases
• Blood Diseases

Cause Classification: Medical


Imperforate Anus

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Imperforate Anus is also known as:
• Anal Atresia
• Anal Membrane
• Anal Stenosis
• Anorectal Malformations
• Ectopic Anus
• High Imperforate Anus
• Low Imperforate Anus
• Perineal Anus
• Rectoperineal Fistula

What is Imperforate Anus?
Imperforate Anus is a rare inborn abnormality characterized by the absence or abnormal localization of the anus. The rectum or the colon may be connected to the vagina or the bladder by a tunnel.

Categories

• Congenital and Genetic Diseases

Cause Classification: Medical


Inclusion-Body Myositis

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

What is Inclusion-Body Myositis?
Inclusion-Body Myositis IBM is one of the inflammatory myopathies, a group of muscle diseases that involves inflammation of the muscles or associated tissues, such as the blood vessels that supply the muscles. A myopathy is a muscle disease, and inflammation is response to cell damage. Inflammatory cells invading muscle tissues is one characteristic of IBM, but the disease is distinct from other inflammatory myopathies in that muscle degeneration also occurs. IBM is named for the clumps of discarded cellular material, the "bodies", that collect in the muscle tissues.

Categories

• Musculoskeletal Diseases
• Nervous System Diseases

Cause Classification: Medical


Incontinentia Pigmenti

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Incontinentia Pigmenti is also known as:
• Bloch-Siemens Incontinentia Pigmenti Melanoblastosis Cutis Linearis
• Bloch-Sulzberger Syndrome
• IP
• Pigmented Dermatosis, Siemens-Bloch Type

What is Incontinentia Pigmenti?
Incontinentia Pigmenti (IP) is a genetic dermatological disorder affecting the skin, hair, teeth, and central nervous system.

Categories

• Congenital and Genetic Diseases
• Eye Diseases
• Mouth Diseases
• Nervous System Diseases
• Skin Diseases

Cause Classification: Medical


Infantile Myofibromatosis

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Infantile Myofibromatosis is also known as:
• Congenital Generalized Fibromatosis
• IM
• Juvenile Myofibromatosis

What is Infantile Myofibromatosis?
Infantile Myofibromatosis is a rare disorder characterized by the growth of one or more benign tumors. The skin, bone, muscle, soft tissue, and, in rare cases, the internal organs can be affected.

Categories

• Congenital and Genetic Diseases
• Nervous System Diseases
• Rare Cancers
• Skin Diseases

Cause Classification: Medical


Inflammatory Arthritis

Awareness Ribbon Color:

Purple and Blue Ribbon for Inflammatory Arthritis

What is Inflammatory Arthritis?
Inflammatory Arthritis is a group of diseases characterized by inflammation of the joints and often other tissues. These include rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, juvenile idiopathic arthritis and systemic lupus erythematosus ((lupus), among others.

Categories

• Autoimmune Diseases
• Autoinflammatory Diseases

Cause Classification: Medical


Inflammatory Bowel Disease

Awareness Ribbon Color:

Purple Ribbon for Inflammatory Bowel Disease

What is Inflammatory Bowel Disease?
Inflammatory Bowel Disease (IBD) is an umbrella term used to describe disorders that involve chronic inflammation of the digestive tract.

Types of IBD include:
• Ulcerative colitis. This condition causes long-lasting inflammation and ulcers in the innermost lining of the large intestine (colon) and rectum.
• Crohn's Disease. This type of IBD is characterized by inflammation of the lining of the digestive tract, which often spreads deep into affected tissues.

Both ulcerative colitis and Crohn's disease usually involve severe diarrhea, abdominal pain, fatigue and weight loss. IBD can be debilitating and sometimes leads to life-threatening complications.

Categories

• Autoimmune Diseases
• Autoinflammatory Diseases
• Digestive Diseases

Cause Classification: Medical


Intermediate Uveitis

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

What is Intermediate Uveitis?
Intermediate Uveitis refers to inflammation localized to the vitreous and peripheral retina.

Categories

• Autoimmune Diseases
• Autoinflammatory Diseases
• Eye Diseases

Cause Classification: Medical


Interstitial Cystitis (IC)

Awareness Ribbon Color:

Teal Ribbon for Interstitial Cystitis

What is Interstitial Cystitis (IC)?
Interstitial Cystitis, also called painful bladder syndrome, is a chronic condition causing bladder pressure, bladder pain and sometimes pelvic pain. The pain ranges from mild discomfort to severe.

Categories

• Kidney and Urinary Diseases
• Not a Rare Disease

Cause Classification: Medical


Intraocular Melanoma, Adult

Awareness Ribbon Color:

Black and Navy Ribbon for Intraocular Melanoma, Adult

What is Intraocular Melanoma, Adult?
Intraocular Melanoma begins in the middle of three layers of the wall of the eye. Intraocular Melanoma is a rare cancer that forms from cells that make melanin in the iris, ciliary body, and choroid. It is the most common eye cancer in adults.

Categories

• Eye Diseases
• Rare Cancers

Cause Classification: Medical
Cross Reference: Cancer Causes And Their Associated Cancer Ribbon Colors


Intraocular Melanoma, Childhood

Awareness Ribbon Color:

Black and Navy Ribbon for Intraocular Melanoma, Childhood
[Gold Cancer Ribbons for Childhood Intraocular Melanoma Awareness][2]

What is Intraocular Melanoma, Childhood?
Intraocular Melanoma in children tends to occur most often in the teenage years as a pigmented tumor involving the choroid or iris.

Categories

• Eye Diseases
• Rare Cancers

Cause Classification: Medical
Cross Reference: Cancer Causes And Their Associated Cancer Color Ribbons


Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

IRF6-Related Disorders is also known as:
• Lip Pits Syndrome

Subdivisions of IRF6-Related Disorders
• Popliteal Pterygium Syndrome
• Van der Woude Syndrome

What is IRF6-Related Disorders?
IRF6-Related Disorders are a group of orofacial clefting disorders including Van der Woude Syndrome (VWS) and Popliteal Pterygium Syndrome (PPS). These conditions are caused by mutations in the interferon regulatory factor 6 (IRF6) gene.

Categories

• Congenital and Genetic Diseases

Cause Classification: Medical


Islet Cell Tumors, Pancreatic Neuroendocrine Tumors

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases
[Purple Cancer Ribbons for Islet Cell Tumor or Pancreatic Neuroendocrine Tumor Awareness][2]

What are Islet Cell Tumors, Pancreatic Neuroendocrine Tumors?
Pancreatic Neuroendocrine Tumors (also known as Islet Cell Tumors or Islet Cell Carcinoma) are a type of neuroendocrine tumor found in the pancreas. Only 5 percent of pancreatic tumors arise in the Islet Cells. The vast majority of tumors found in the pancreas are adenocarcinoma, which is more commonly referred to as Pancreatic Cancer.

Categories

• Rare Tumors

Cause Classification: Medical
Cross Reference: Cancer Causes And Their Associated Cancer Ribbon Colors


Ivemark Syndrome

Awareness Ribbon Color:

Zebra Ribbon for Rare Diseases

Ivemark Syndrome is also known as:
• Asplenia Syndrome
• Asplenia with Cardiovascular Anomalies
• Bilateral Right-Sidedness Sequence
• Right Isomerism Sequence

What is Ivemark Syndrome?
Ivemark Syndrome is a rare disorder that affects multiple organ systems of the body. It is characterized by the absence or underdevelopment of the spleen, malformations of the heart and the abnormal arrangement of the internal organs of the chest and abdomen.

Categories

• Congenital and Genetic Diseases
• Heart Diseases
• Kidney and Urinary Diseases

Cause Classification: Medical