syndrome
set of medical signs and symptoms which are correlated with each other and often clinically associated with a particular disease or disorder
Van den Ende-Gupta syndrome
Van den Ende-Gupta syndrome is a very rare syndrome characterized by blepharophimosis, arachnodactyly, joint contractures, and characteristic dysmorphic features
achalasia microcephaly syndrome
Human disease
meningeal syndrome
clinical syndrome
Pierson syndrome
Pierson syndrome is characterised by the association of congenital nephrotic syndrome and ocular anomalies with microcoria
dysentery
inflammation of the intestine causing diarrhea with blood
fragile X syndrome
congenital disorder of nervous system
subclavian steal syndrome
constellation of signs and symptoms that arise from retrograde (reversed) blood flow in the vertebral artery or the internal thoracic artery, due to a proximal stenosis (narrowing) and/or occlusion of the subclavian artery
Werner syndrome
Lethal autosomal recessive disorder
popliteal pterygium syndrome
Human disease
superior mesenteric artery syndrome
gastro-vascular disorder in which the third and final portion of the duodenum is compressed between the abdominal aorta (AA) and the overlying superior mesenteric artery
sternal angle
synarthrotic joint formed by the articulation of the manubrium and the body of the sternum
diarrhetic shellfish poisoning
syndrome of shellfish poisoning
hand-foot-genital syndrome
autosomal dominant human genetic disease characterized by limb malformations (e.g. bilateral shortening of thumbs/big toes) and urogenital defects (e.g. abnormalities of ureters/urethra; incomplete Müllerian fusion in females; hypospadias in males)
akinetic-rigid syndrome
syndrome
akinetic-rigid syndrome
syndrome
pseudo-TORCH syndrome
autosomal recessive disease that is characterized by congenital microcephaly, intracranial calcifications, severe developmental delay, severe developmental delay, simplified gyration and polymicrogyria
Celibacy syndrome
media hypothesis
LADD syndrome
autosomal dominant disease that is characterized by abnormalities affecting the lacrimal and salivary glands and ducts, ears, teeth and fingers and toes
cataract-intellectual disability-hypogonadism syndrome
This syndrome is characterized by the association of intellectual deficit, congenital cataract, and hypogonadotropic hypogonadism
Adie-Critchley syndrome
neurological syndrome
Neck-tongue syndrome
medical disorder
shock
medical condition of insufficient blood flow to the tissues of the body
Roberts syndrome
Human disease
hepatic encephalopathy
brain disease that is characterized by loss of brain function, the occurrence of confusion, altered level of consciousness, and coma that results when the liver is unable to remove toxins from the blood
TAR syndrome
genetic disorder
Wolfram syndrome
rare disease in which a human simultaneously has diabetes insipidus, diabetes, optic nerve atrophy and deafness syndrome
parkinsonian syndrome
symptoms that resemble Parkinson's disease
Miller syndrome
human disease
amnesic shellfish poisoning
syndrome of shellfish poisoning
dysplastic nevus syndrome
Human skin disease
FACES syndrome
human disease
Warburg micro syndrome
autosomal recessive disease characterized by severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis or hypoplasia of the corpus callosum and hypogenitalism
pervasive refusal syndrome
Hypothesized pediatric mental disorder
Sensenbrenner syndrome
Human disease
triple-A syndrome
Human disease
CHIME syndrome
CHIME syndrome is a rare ectodermal dysplasia syndrome characterized by ocular colobomas, cardiac defects, ichthyosiform dermatosis, intellectual disability, conductive hearing loss and epilepsy
Small Penis Syndrome
unreasonable belief that the penis size is below normal
Child vehicular heat stroke deaths
phenomenon in which children are mistakenly left in vehicles
Fowler syndrome
human disease
Warsaw breakage syndrome
Human disease
Havana syndrome
set of medical symptoms affecting U.S. and Canada government personnel
Kenny-Caffey syndrome
genetic condition characterized by long bone sclerosis and thickening, short stature, and head and eye anomalies. Many affected individuals have hypoparathyroidism with hypocalcemia