Directory
Inclusion myopathy 2
Inclusion myopathy 2 (IM2) is a rare inherited disorder that belongs to the group of myopathies. It is a chronic condition that is characterized by...
Infantile hyperglycemia
Infantile hyperglycemia is a condition characterized by elevated blood glucose levels in newborns and infants. It can...
Inappropriate sinus tachycardia (IST)
Inappropriate sinus tachycardia (IST) is a condition characterized by an abnormally increased heart rate.
Incontinence of pigment
Incontinentia pigmenti, also known as vitiligo, is a dermatological disorder characterized by the gradual loss of...
Imperforate anus
Imperforate anus, or anal atresia, is a serious developmental disorder characterized by the absence of normal o...
Low Calcium in Babies
Low calcium levels in infants, also known as hypocalcemia, is a condition characterized by a decrease in the end...
Kaufman's oculocerebrofacial syndrome
Kaufman oculocerebrofacial syndrome is a rare genetic disorder that belongs to a group of syndromes characterized by multiple...
Jock itch
Jock itch is a fungal infection caused by dermatophytes that occurs in the groin, buttocks, and inter...
Primary osteoporosis in children
Primary osteoporosis in children is a disease characterized by decreased bone mass and microarchitectural deterioration of the bone...
Increased intracranial pressure
Increased intracranial pressure (ICP) is a pathological condition characterized by increased fluid pressure, ...
Hearing Loss in Infants
Hearing loss in infants is a serious medical problem that can significantly impact a child's development. It...
Interrupted aortic arch
An interrupted aortic arch is a developmental anomaly characterized by the presence of a defect in the arterial arch of the aorta, which leads to a disruption of...
Industrial bronchitis
Industrial bronchitis is a chronic inflammatory disease of the bronchi caused by prolonged exposure to adverse...
The Jumping Frenchmen of Maine
Jumping Frenchmen of Maine, also known as "Maine disease," is a rare and mysterious disorder characterized by...
Colon cancer
Colon cancer is a malignant neoplasm that develops in the tissues of the large or small intestine, most often in the rectum or colon...
Indigestion
An upset stomach is a condition characterized by a disruption of the digestive system. It can manifest itself as ...
Kaposi's sarcoma
Kaposi's sarcoma (KS) is a malignant neoplasm arising from vascular cells and characterized by the development of ...
IPEX syndrome
IPEX syndrome (Immune dysregulation, Polyendocrinopathy, Enteropathy, X-linked) is a rare genetic disorder characterized by...
Isaacs syndrome
Isaacs syndrome, better known as generalized myoclonic epileptic syndrome, is a rare neurological ...
Jalili syndrome
Jalili syndrome is a rare genetic disorder that belongs to a group of diseases caused by a combination of functional and structural...
Jackson-Weiss syndrome
Jackson-Weiss syndrome (JWS) is a rare genetic disorder that belongs to the category of craniofacial dysplasia syndromes. It is...
Jervell Lange-Nielsen syndrome (JLNS)
Jervell Lange-Nielsen syndrome (JLNS) is a rare genetic disorder characterized by the combination of a long QT interval on the e...
Jones syndrome
Jones syndrome is a rare genetic disorder characterized by impaired kidney function and a tendency to develop chronic kidney disease.
Joubert syndrome
Joubert syndrome, also known as nonspecific progressive chorioretinopathy, is an inherited disorder characterized by...
Johanson-Blizzard syndrome
Johanson-Blizzard syndrome (JBS) is a rare genetic disorder characterized by a variety of abnormalities, both facial...
KBG syndrome
KBG syndrome (Kunta-Barney and Goodman syndrome) is a rare genetic disorder characterized by specific physical...
Kabuki syndrome
Kabuki syndrome (or Kabuki-macrosomia syndrome) is a rare genetic disorder characterized by a unique set of physical...
Kallmann syndrome
Kallmann syndrome is a rare inherited disorder characterized by a combination of hypogonadism and anosmia, which is a decrease or loss of...
Kartagener's syndrome
Kartagener syndrome is a rare genetic disorder that belongs to a group of primary disorders of the ciliary structure, characterized by...
Keitel syndrome
Keitel syndrome (or Keitel-Lefevre syndrome) is a rare inherited disorder characterized by a combination of neurological...
