Noonan syndrome with multiple lentigines
Also known as Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome, Cardiomyopathic lentiginosis, Gorlin syndrome II, LEOPARD syndrome+8 more
Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome, Cardiomyopathic lentiginosis, Gorlin syndrome II, LEOPARD syndrome, familial multiple lentigines syndrome, generalised lentiginosis, generalized lentiginosis, lentigines, electrocardiographic conduction defects, 0cular hypertelorism, pulmonary stenosis, abnormalities of the genitals, retarded Growth, deafness, lentiginosis profusa syndrome, progressive cardiomyopathic lentiginosis, Moynahan syndrome, lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonic stenosis, abnormal genitalia, retardation of growth, Deafnes.
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An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome, Cardiomyopathic lentiginosis, Gorlin syndrome II, LEOPARD syndrome, familial multiple lentigines syndrome, generalised lentiginosis, generalized lentiginosis, lentigines, electrocardiographic conduction defects, 0cular hypertelorism, pulmonary stenosis, abnormalities of the genitals, retarded Growth, deafness, lentiginosis profusa syndrome, progressive cardiomyopathic lentiginosis, Moynahan syndrome, lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonic stenosis, abnormal genitalia, retardation of growth, Deafnes
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.