Disease Index
9,486 diseasescongenital pulmonary airway malformation type 3
human disease
congenital pulmonary airway malformation type 4
human disease
congenital pulmonary lymphangiectasia
Congenital pulmonary lymphangiectasia (PL) is a rare developmental disorder involving the lung and characterized by pulmonary subpleural, interlobar, perivascular, and peribronchial lymphatic dilatation
MeSH: C537727
congenital pulmonary veins anomaly
Aberrant drainage of one or more of the pulmonary veins which causes the return of oxygen-rich blood to the right atrium
congenital pulmonary veins atresia or stenosis
congenital pulmonary venous return anomaly
TAPVC
ICD: Q26.2
Congenital radial head dislocation
human disease
congenital renal artery stenosis
human disease
congenital retinal arteriovenous communication
human disease
congenital rubella syndrome
human disease
ICD: P35.0MeSH: D012410
congenital secondary polycythemia
human disease
congenital secretory chloride diarrhea 1
secretory diarrhea that has material basis in mutation in the SLC26A3 gene
MeSH: C536210
congenital secretory sodium diarrhea 3
secretory diarrhea that has material basis in homozygous or compound heterozygous mutation in the SPINT2 gene on chromosome 19q13
congenital secretory sodium diarrhea 8
secretory diarrhea that has material basis in homozygous or compound heterozygous mutation in the SLC9A3 gene on chromosome 5p15
Congenital self-healing reticulohistiocytosis
Hashimoto-Pritzker histiocytosis (HPH) is a variant of Langerhans cell histiocytosis (see this term) characterized by multiple disseminated skin lesions (firm, red-brown, painless papulo-nodules)
MeSH: C535843
congenital short bowel syndrome
congenital shoulder dislocation
human disease
congenital sialidosis type 2
human disease
congenital smooth muscle hamartoma
medical condition
congenital stationary night blindness
night blindness that is characterized by hemeralopia with a moderate loss of visual acuity and caused by defective photoreceptor-to-bipolar cell signaling with common ERG findings of reduced or absent b-waves and generally normal a-waves
MeSH: C537743
congenital stenosis of the inferior vena cava
human disease
congenital stromal corneal dystrophy
Human disease
MeSH: C566452
congenital subglottic stenosis
human disease
congenital sucrase-isomaltase deficiency with minimal starch tolerance
human disease
congenital sucrase-isomaltase deficiency with starch and lactose intolerance
human disease
congenital sucrase-isomaltase deficiency with starch intolerance
human disease
congenital sucrase-isomaltase deficiency without starch intolerance
human disease
congenital sucrase-isomaltase deficiency without sucrose intolerance
human disease
congenital supravalvular mitral ring
human disease
congenital symblepharon
human disease