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K-P-R is a Semitic root, in Arabic and Hebrew rendered as K-F-R (Arabic: ك-ف-ر; Hebrew: כ-פ-ר).The basic meaning of the root is "to cover", but it is used in the sense "to conceal" and hence "to deny", and its notability derives from its use for religious heresy or apostasy (as it were describing the "concealment" of religious truth) in both Islam and Judaism.
Particular to the Qalandari genre of poetry are items that refer to their practices of gambling, games, consuming intoxicants, syncreticism, libertinism, antinomialism, violating societal norms and Nazar ila'l-murd, things commonly referred to as Kufr or Khurafat by orthodox Muslims. The order was often viewed with scrutiny by Islamic authorities.
In Islam, the munafiqun ('hypocrites', Arabic: منافقون, singular منافق munāfiq) or false Muslims or false believers are a group decried in the Quran as outward Muslims who were inwardly concealing disbelief ("kufr") and actively sought to undermine the Muslim community. [1]
Starting with Google Chrome 4.1, the application added a built-in translation bar using Google Translate. Language translation is currently available for 52 languages. [ 78 ] When Chrome detects a foreign language other than the user's preferred language set during the installation time, it asks the user whether or not to translate.
The Arabic terms kufr ("unbelief") and kāfir ("unbeliever"), alongside other terms employing the same triliteral root k-f-r, are found both in the Quran and the ḥadīth literature, but the term takfīr used to declare another Muslim as kāfir is found in neither. [4] "
The influence of this led to the transformation of the concept of kufr in later Sunni theology; in addition to unbelief, kufr acquired the meaning of heterodoxy and heresy. [192] In the view of Watt, the Kharijite insistence on the rule according to the Qur'an prevented the early Muslim empire from turning into a purely secular Arab state.
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Kufor–Rakeb syndrome is associated with mutations in the ATP13A2 gene. [8] The inheritance pattern for KRS is autosomal recessive. [9] If a male and female carrier, who each have one mutation in ATP13A2 have a child, there is a 25% chance the child has KRS, a 50% chance the child is a carrier for KRS, and a 25% chance the child does not have KRS.