Faster access than browser!
69 relations: Absence of gluteal muscle, Ameloblastic fibroma, Angiomyolipoma, Ashish Suri, Bannayan–Riley–Ruvalcaba syndrome, Basaloid follicular hamartoma, Benign tumor, Bile duct hamartoma, Bone tumor, Breast cancer classification, Brunner's glands, Calcification, Chest radiograph, Childhood disintegrative disorder, Chorangioma, Choristoma, Comedo, Congenital melanocytic nevus, Cowden syndrome, Cronkhite–Canada syndrome, Desmoplastic trichoepithelioma, Eccrine angiomatous hamartoma, Eugen Albrecht, Fibrous hamartoma of infancy, Folliculosebaceous cystic hamartoma, Frontal lobe epilepsy, Gastrointestinal disease, Gelastic seizure, Genomic Medicine Institute, GLI2, Gynecomastia, Hamartia (medical term), Heart cancer, Hemimegalencephaly, Hereditary breast–ovarian cancer syndrome, Heterochromia iridum, Index of oncology articles, Johanson–Blizzard syndrome, Judith Goslin Hall, Juvenile polyposis syndrome, Leiomyomatous hamartoma, Lhermitte–Duclos disease, Lisch nodule, List of cutaneous conditions, List of diseases (F), List of ICD-9 codes 740–759: congenital anomalies, List of MeSH codes (C04), Liver tumor, Lung cancer, Manuel Belgrano, ..., Meckel's diverticulum, Melanocytic nevus, Meningioangiomatosis, Mucinous nevus, Multiple hamartoma syndrome, Odontoma, Peutz–Jeghers syndrome, Polycystic liver disease, Polyp (medicine), Presacral space, PTEN (gene), Respiratory disease, SDHD, Small intestine cancer, Solitary pulmonary nodule, Splenomegaly, Tongue disease, Tuber cinereum hamartoma, Tuberous sclerosis. Expand index (19 more) »
Absence of gluteal muscle
The congenital absence of the gluteal muscle was described in 1976, as occurring in a brother and sister with absence of gluteal muscles and with spina bifida occulta.
New!!: Hamartoma and Absence of gluteal muscle · See more »
Ameloblastic fibroma
An ameloblastic fibroma is a fibroma of the ameloblastic tissue, that is, an odontogenic tumor arising from the enamel organ or dental lamina.
New!!: Hamartoma and Ameloblastic fibroma · See more »
Angiomyolipoma
Angiomyolipomas are the most common benign tumour of the kidney.
New!!: Hamartoma and Angiomyolipoma · See more »
Ashish Suri
Ashish Suri (born April 8, 1970) is an Indian neurosuregeon, medical academic and a professor at the Department of Neurosurgery of the All India Institute of Medical Sciences, Delhi.
New!!: Hamartoma and Ashish Suri · See more »
Bannayan–Riley–Ruvalcaba syndrome
Bannayan–Riley–Ruvalcaba syndrome (BRRS) is a rare overgrowth syndrome and hamartomatous disorder with occurrence of multiple subcutaneous lipomas, macrocephaly and hemangiomas.
New!!: Hamartoma and Bannayan–Riley–Ruvalcaba syndrome · See more »
Basaloid follicular hamartoma
A basaloid follicular hamartoma is a cutaneous condition characterized as distinctive benign adnexal tumor that has several described variants.
New!!: Hamartoma and Basaloid follicular hamartoma · See more »
Benign tumor
A benign tumor is a mass of cells (tumor) that lacks the ability to invade neighboring tissue or metastasize.
New!!: Hamartoma and Benign tumor · See more »
Bile duct hamartoma
A bile duct hamartoma or biliary hamartoma, is a benign tumour-like malformation of the liver.
New!!: Hamartoma and Bile duct hamartoma · See more »
Bone tumor
A bone tumor (also spelled bone tumour) is a neoplastic growth of tissue in bone.
New!!: Hamartoma and Bone tumor · See more »
Breast cancer classification
Breast cancer classification divides breast cancer into categories according to different schemes criteria and serving a different purpose.
New!!: Hamartoma and Breast cancer classification · See more »
Brunner's glands
Brunner's glands (or duodenal glands) are compound tubular submucosal glands found in that portion of the duodenum which is above the hepatopancreatic sphincter (a.k.a. sphincter of Oddi).
New!!: Hamartoma and Brunner's glands · See more »
Calcification
Calcification is the accumulation of calcium salts in a body tissue.
New!!: Hamartoma and Calcification · See more »
Chest radiograph
A chest radiograph, colloquially called a chest X-ray (CXR), or chest film, is a projection radiograph of the chest used to diagnose conditions affecting the chest, its contents, and nearby structures.
New!!: Hamartoma and Chest radiograph · See more »
Childhood disintegrative disorder
The childhood disintegrative disorder (CDD), also known as Heller's syndrome and disintegrative psychosis, is a rare condition characterized by late onset of developmental delays—or severe and sudden reversals—in language, social function, and motor skills.
New!!: Hamartoma and Childhood disintegrative disorder · See more »
Chorangioma
A chorangioma is a non-neoplastic, hamartoma-like growth in the placenta consisting of blood vessels.
New!!: Hamartoma and Chorangioma · See more »
Choristoma
Choristomas, forms of heterotopia, are closely related benign tumors, found in abnormal locations.
New!!: Hamartoma and Choristoma · See more »
Comedo
A comedo is a clogged hair follicle (pore) in the skin.
New!!: Hamartoma and Comedo · See more »
Congenital melanocytic nevus
The congenital melanocytic nevus is a type of melanocytic nevus (or mole) found in infants at birth.
New!!: Hamartoma and Congenital melanocytic nevus · See more »
Cowden syndrome
Cowden syndrome (also known as Cowden's disease and multiple hamartoma syndrome) is an autosomal dominant inherited condition characterized by benign overgrowths called hamartomas as well as an increased lifetime risk of breast, thyroid, uterine, and other cancers.
New!!: Hamartoma and Cowden syndrome · See more »
Cronkhite–Canada syndrome
Cronkhite–Canada syndrome is a rare syndrome characterized by multiple polyps of the digestive tract.
New!!: Hamartoma and Cronkhite–Canada syndrome · See more »
Desmoplastic trichoepithelioma
A desmoplastic trichoepithelioma is a cutaneous condition characterized by a solitary, firm skin lesion on the face.
New!!: Hamartoma and Desmoplastic trichoepithelioma · See more »
Eccrine angiomatous hamartoma
Eccrine angiomatous hamartoma usually appear as a solitary nodular lesion on the acral areas of the extremities, particularly the palms and soles.
New!!: Hamartoma and Eccrine angiomatous hamartoma · See more »
Eugen Albrecht
Eugen Albrecht (21 June 1872, in Sonthofen – 18 June 1908, in Frankfurt am Main) was a German pathologist.
New!!: Hamartoma and Eugen Albrecht · See more »
Fibrous hamartoma of infancy
Fibrous hamartoma of infancy is a rapidly growing, painless, ill-defined subcutaneous or intradermal nodule that is generally solitary and less than 5 cm in size, though, rarely, multiple lesions occur synchronously.
New!!: Hamartoma and Fibrous hamartoma of infancy · See more »
Folliculosebaceous cystic hamartoma
Folliculosebaceous cystic hamartoma abbreviated as (FSCH) is a rare cutaneous hamartoma consisting of dilated folliculosebaceous units invested in mesenchymal elements.
New!!: Hamartoma and Folliculosebaceous cystic hamartoma · See more »
Frontal lobe epilepsy
Frontal lobe epilepsy, or FLE, is a neurological disorder that is characterized by brief, recurring seizures that arise in the frontal lobes of the brain, often while the patient is sleeping.
New!!: Hamartoma and Frontal lobe epilepsy · See more »
Gastrointestinal disease
Gastrointestinal diseases refer to diseases involving the gastrointestinal tract, namely the esophagus, stomach, small intestine, large intestine and rectum, and the accessory organs of digestion, the liver, gallbladder, and pancreas.
New!!: Hamartoma and Gastrointestinal disease · See more »
Gelastic seizure
A gelastic seizure, also known as "gelastic epilepsy", is a rare type of seizure that involves a sudden burst of energy, usually in the form of laughing or crying.
New!!: Hamartoma and Gelastic seizure · See more »
Genomic Medicine Institute
The Genomic Medicine Institute at the Cleveland Clinic is an inter-disciplinary institute and department that focuses on patient care, patient-oriented research, and outreach and education in personalized healthcare guided by genetics and genomics.
New!!: Hamartoma and Genomic Medicine Institute · See more »
GLI2
Zinc finger protein GLI2 also known as GLI family zinc finger 2 is a protein that in humans is encoded by the GLI2 gene.
New!!: Hamartoma and GLI2 · See more »
Gynecomastia
Gynecomastia is an endocrine system disorder in which a noncancerous increase in the size of male breast tissue occurs.
New!!: Hamartoma and Gynecomastia · See more »
Hamartia (medical term)
A hamartia is a focal malformation consisting of disorganized arrangement of tissue types that are normally present in the anatomical area.
New!!: Hamartoma and Hamartia (medical term) · See more »
Heart cancer
Heart cancer is an extremely rare form of cancer that is divided into primary tumors of the heart and secondary tumors of the heart.
New!!: Hamartoma and Heart cancer · See more »
Hemimegalencephaly
Hemimegalencephaly (HME), or unilateral megalencephaly, is a rare congenital disorder affecting all or a part of a cerebral hemisphere.
New!!: Hamartoma and Hemimegalencephaly · See more »
Hereditary breast–ovarian cancer syndrome
Hereditary breast–ovarian cancer syndromes (HBOC) are cancer syndromes that produce higher than normal levels of breast cancer and ovarian cancer in genetically related families (either one individual had both, or several individuals in the pedigree had one or the other disease).
New!!: Hamartoma and Hereditary breast–ovarian cancer syndrome · See more »
Heterochromia iridum
Heterochromia is a difference in coloration, usually of the iris but also of hair or skin.
New!!: Hamartoma and Heterochromia iridum · See more »
Index of oncology articles
This is a list of terms related to oncology.
New!!: Hamartoma and Index of oncology articles · See more »
Johanson–Blizzard syndrome
Johanson–Blizzard syndrome (JBS) is a rare, sometimes fatal autosomal recessive multisystem congenital disorder featuring abnormal development of the pancreas, nose and scalp, with mental retardation, hearing loss and growth failure.
New!!: Hamartoma and Johanson–Blizzard syndrome · See more »
Judith Goslin Hall
Judith Goslin Hall, (born July 3, 1939) is a pediatrician, clinical geneticist and dysmorphologist who is a dual citizen of the United States and Canada.
New!!: Hamartoma and Judith Goslin Hall · See more »
Juvenile polyposis syndrome
Juvenile polyposis syndrome is a syndrome characterized by the appearance of multiple juvenile polyps in the gastrointestinal tract.
New!!: Hamartoma and Juvenile polyposis syndrome · See more »
Leiomyomatous hamartoma
Leiomyomatous hamartoma is a hamartoma which appears as a painless, soft polypoid (polyp-like) mass.
New!!: Hamartoma and Leiomyomatous hamartoma · See more »
Lhermitte–Duclos disease
Lhermitte–Duclos disease (LDD), also called dysplastic gangliocytoma of the cerebellum, is a rare, slowly growing tumor of the cerebellum, a gangliocytoma sometimes considered to be a hamartoma, characterized by diffuse hypertrophy of the granular layer of the cerebellum.
New!!: Hamartoma and Lhermitte–Duclos disease · See more »
Lisch nodule
Lisch nodule, also known as iris hamartoma, is a pigmented hamartomatous nodular aggregate of dendritic melanocytes affecting the iris, named after Austrian ophthalmologist Karl Lisch (1907–1999), who first recognized them in 1937.
New!!: Hamartoma and Lisch nodule · See more »
List of cutaneous conditions
Many conditions affect the human integumentary system—the organ system covering the entire surface of the body and composed of skin, hair, nails, and related muscle and glands.
New!!: Hamartoma and List of cutaneous conditions · See more »
List of diseases (F)
This is a list of diseases starting with the letter "F".
New!!: Hamartoma and List of diseases (F) · See more »
List of ICD-9 codes 740–759: congenital anomalies
14.
New!!: Hamartoma and List of ICD-9 codes 740–759: congenital anomalies · See more »
List of MeSH codes (C04)
The following is a list of the "C" codes for MeSH.
New!!: Hamartoma and List of MeSH codes (C04) · See more »
Liver tumor
Liver tumors or hepatic tumors are tumors or growths on or in the liver (medical terms pertaining to the liver often start in hepato- or hepatic from the Greek word for liver, hepar).
New!!: Hamartoma and Liver tumor · See more »
Lung cancer
Lung cancer, also known as lung carcinoma, is a malignant lung tumor characterized by uncontrolled cell growth in tissues of the lung.
New!!: Hamartoma and Lung cancer · See more »
Manuel Belgrano
Manuel José Joaquín del Corazón de Jesús Belgrano y González (3 June 1770 – 20 June 1820), usually referred to as Manuel Belgrano, was an Argentine economist, lawyer, politician, and military leader.
New!!: Hamartoma and Manuel Belgrano · See more »
Meckel's diverticulum
A Meckel's diverticulum, a true congenital diverticulum, is a slight bulge in the small intestine present at birth and a vestigial remnant of the omphalomesenteric duct (also called the vitelline duct or yolk stalk).
New!!: Hamartoma and Meckel's diverticulum · See more »
Melanocytic nevus
A melanocytic nevus (also known as nevocytic nevus, nevus-cell nevus and commonly as a mole) is a type of melanocytic tumor that contains nevus cells.
New!!: Hamartoma and Melanocytic nevus · See more »
Meningioangiomatosis
Meningioangiomatosis is a rare disease of the brain.
New!!: Hamartoma and Meningioangiomatosis · See more »
Mucinous nevus
Mucinous nevus (also known as "Nevus mucinosus") is a rare cutaneous condition characterized by hamartoma that can be congenital or acquired.
New!!: Hamartoma and Mucinous nevus · See more »
Multiple hamartoma syndrome
Multiple hamartoma syndrome is a syndrome characterized by more than one hamartoma.
New!!: Hamartoma and Multiple hamartoma syndrome · See more »
Odontoma
An odontoma (also termed odontome) is a benign tumour of odontogenic origin (i.e. linked to tooth development).
New!!: Hamartoma and Odontoma · See more »
Peutz–Jeghers syndrome
Peutz–Jeghers syndrome (often abbreviated PJS) is an autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa (melanosis).
New!!: Hamartoma and Peutz–Jeghers syndrome · See more »
Polycystic liver disease
Polycystic liver disease (PLD) usually describes the presence of multiple cysts scattered throughout normal liver tissue.
New!!: Hamartoma and Polycystic liver disease · See more »
Polyp (medicine)
A polyp is an abnormal growth of tissue projecting from a mucous membrane.
New!!: Hamartoma and Polyp (medicine) · See more »
Presacral space
In human anatomy, the presacral space is inside the pelvis, behind the rectum and in front of the coccyx and sacrum.
New!!: Hamartoma and Presacral space · See more »
PTEN (gene)
Phosphatase and tensin homolog (PTEN) is a protein that, in humans, is encoded by the PTEN gene.
New!!: Hamartoma and PTEN (gene) · See more »
Respiratory disease
Respiratory disease is a medical term that encompasses pathological conditions affecting the organs and tissues that make gas exchange possible in higher organisms, and includes conditions of the upper respiratory tract, trachea, bronchi, bronchioles, alveoli, pleura and pleural cavity, and the nerves and muscles of breathing.
New!!: Hamartoma and Respiratory disease · See more »
SDHD
Succinate dehydrogenase cytochrome b small subunit, mitochondrial (CybS), also known as succinate dehydrogenase complex subunit D (SDHD), is a protein that in humans is encoded by the SDHD gene.
New!!: Hamartoma and SDHD · See more »
Small intestine cancer
In oncology, small intestine cancer, also small bowel cancer and cancer of the small bowel, is a cancer of the small intestine.
New!!: Hamartoma and Small intestine cancer · See more »
Solitary pulmonary nodule
A solitary pulmonary nodule (SPN) or coin lesion is a mass in the lung smaller than 3 centimeters in diameter.
New!!: Hamartoma and Solitary pulmonary nodule · See more »
Splenomegaly
Splenomegaly is an enlargement of the spleen.
New!!: Hamartoma and Splenomegaly · See more »
Tongue disease
Tongue diseases can be congenital or acquired, and are multiple in number.
New!!: Hamartoma and Tongue disease · See more »
Tuber cinereum hamartoma
Tuber cinereum hamartoma (also known as hypothalamic hamartoma) is a benign tumor in which a disorganized collection of neurons and glia accumulate at the tuber cinereum of the hypothalamus on the floor of the third ventricle.
New!!: Hamartoma and Tuber cinereum hamartoma · See more »
Tuberous sclerosis
Tuberous sclerosis, or tuberous sclerosis complex (TSC), or epiloia (acronym of "epilepsy, low intelligence, adenoma sebaceum"), is a rare multisystem genetic disease that causes benign tumors to grow in the brain and on other vital organs such as the kidneys, heart, liver, eyes, lungs, and skin.
New!!: Hamartoma and Tuberous sclerosis · See more »
Redirects here:
Fibrolipomatosis, Generalised follicular hamartoma, Hamartomas, Hamartomatous, Hamartomatous lesion, Hamartoses, Macrodactylia fibrolipomatosis, Macrodystrophy lipomatosa.
References
[1] https://en.wikipedia.org/wiki/Hamartoma
