Disease Index
9,486 diseasesphosphoribosylaminoimidazole carboxylase deficiency
human disease
phosphoribosylpyrophosphate synthetase superactivity
human disease
MeSH: C567064
photodermatosis
medical condition
ICD: L56.8
photosensitive epilepsy
epilepsy characterized by seizures triggered by visual stimuli that form patterns in space or time, such as flashing lights
phyllodes tumor
medical condition
ICD: C50MeSH: D003557
PIBIDS syndrome
Pickardt syndrome
Rare form of tertiary hypothyroidism
ICD: E23
piebald trait-neurologic defects syndrome
human disease
MeSH: C536955
piebaldism
human disease
MeSH: D016116
Pierpont syndrome
human disease
MeSH: C566559
Pierre Robin syndrome
a congenital condition with micrognathia and glossoptosis
ICD: Q87.0MeSH: D010855
Pierre robin syndrome associated with a chromosomal anomaly
human disease
Pierre robin syndrome associated with bone disease
human disease
Pierre robin syndrome associated with branchial archs anomalies
human disease
Pierre robin syndrome associated with collagen disease
human disease
Pierre robin syndrome-faciodigital anomaly syndrome
medical condition
MeSH: C535926
Pierson syndrome
Pierson syndrome is characterised by the association of congenital nephrotic syndrome and ocular anomalies with microcoria
MeSH: C537185
pigment dispersion syndrome
eye disease characterized by slit-like depigmented areas of the iris with up to 50% of patients going on to develop gluacoma
MeSH: C563184
pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome
human disease
pigmentation disorder
human or animal skin condition
ICD: L81MeSH: D010859
pigmentation disorder with eye involvement
human disease
pigmentation disorder with eye involvement, excluding albinism
human disease
pigmented conjunctival lesion
human disease
pigmented palpebral tumor
human disease
pigmented paravenous retinochoroidal atrophy
pigmented villonodular synovitis
human disease
MeSH: D013586
Pili annulati
medical condition
ICD: Q84.1MeSH: C537187
Pili bifurcati
medical condition
ICD: L67.8
Pili multigemini
medical condition
MeSH: C537188
pili torti
medical condition
ICD: Q84.1MeSH: C562485