Disease Index
9,486 diseasesposterior fusion of lumbosacral vertebrae-blepharoptosis syndrome
Posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome is characterized by congenital ptosis and posterior fusion of the lumbosacral vertebrae. It has been described in a mother and her two daughters.
MeSH: C536344
posterior hypospadias
posterior meningocele
posterior polymorphous corneal dystrophy
Human disease
MeSH: C562745
posterior urethral valve
congenital disorder of urinary system
ICD: Q64.2
posterior uveitis
Human disease
MeSH: D015866
postinfectious autoimmune disease with chorea
human disease
postinfectious encephalitis
human disease
postinfectious vasculitis
human disease
postlingual non-syndromic genetic deafness
human disease
postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome
human disease
postorgasmic illness syndrome
human disease
postpartum psychosis
abrupt onset of psychotic symptoms shortly following childbirth
ICD: F53.1
postsynaptic congenital myasthenic syndrome
human disease
posttransplant acute limbic encephalitis
human disease
postural orthostatic tachycardia syndrome
condition in which a change from lying to standing causes an abnormally large increase in heart rate
MeSH: D054972
potassium-aggravated myotonia
human disease
MeSH: C538353
Potocki-Luspski syndrome
chromosomal duplication syndrome characterized by hypotonia, failure to thrive, mental retardation, pervasive developmental disorders and congenital anomalies that has material basis in duplication of a region of chromosome 17p11.2
MeSH: C536578
Potocki–Shaffer syndrome
human disease
MeSH: C538356
pouchitis
Acute inflammation in the intestinal mucosa of the continent ileal reservoir (or pouch) in patients who have undergone ileostomy and restorative proctocolectomy (proctocolectomy, restorative)
MeSH: D019449
PPoma
Prader-Willi syndrome due to imprinting mutation
human disease
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
human disease
Prader-Willi syndrome due to paternal 15q11q13 deletion
human disease
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
human disease
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2
human disease
Prader-Willi syndrome due to point mutation
human disease
Prader-Willi syndrome due to translocation
human disease
Prader-Willi-like syndrome
human disease
Prader-Willi-like syndrome due to point mutation
human disease